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Assay Purity & Pharmacopoeial Grade Sodium Stearyl Fumarate (SSF) â Low Nitrite Grade is an excipient lubricant developed to meet low nitrite specifications for sensitive tablet formulations. It provides lubrication benefits similar to other stearate lubricants while addressing nitrite-sensitive regulatory or formulation constraints. SSF is widely used in direct compression and tableting workflows requiring controlled impurity profiles. Composition & Physicochemical Properties SSF is a fumarate-based sodium stearate salt supplied to low-nitrite standards where inputs specify reduced nitrite levels. It is handled and packaged to avoid contamination and moisture ingress. Buyers select this grade when nitrite limits are a formulation or regulatory concern and when consistent batch impurity profiles are required.
Min. Order: 1 Unit
GST
Assay Purity & Pharmacopoeial Grade Microcrystalline Cellulose (MCC) â Low Nitrite Grade is selected for tablet formulations that require controlled impurity profiles. MCC is widely used as a filler and binder in direct compression and wet granulation processes. Low nitrite variants are specified when formulation or regulatory constraints necessitate reduced nitrite content. Composition & Physicochemical Properties MCC is supplied as a consistent cellulose powder with defined particle characteristics to support predictable compaction and dissolution. Packaging protects against moisture and ensures handling ease in production lines. Buyers evaluate MCC grades for compressibility and blend performance.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Co-Processed Microcrystalline Cellulose (Co-Processed MCC) combines microcrystalline cellulose with functional excipients to provide improved binding, flow, and compression performance. It is designed for direct compression and dry granulation processes to reduce formulation complexity and improve tablet robustness. Procurement groups source co-processed MCC to shorten development timelines and simplify supply chains for high-speed production. Composition & Physicochemical Properties Co-Processed MCC is a blended excipient with controlled particle characteristics and improved flowability. It reduces the need for multiple excipient additions and is compatible with many active pharmaceutical ingredients when evaluated for specific dissolution and stability requirements. Packaging protects the powder from moisture and facilitates on-line dosing.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Magnesium Stearate â Low Nitrite Grade is used where nitrite control is required alongside conventional lubrication in tablet manufacturing. It reduces die friction and improves ejection behaviour while supporting stricter impurity limits that may be required by certain formulations. Formulators and QA teams commonly request low nitrite grades for sensitive active combinations. Composition & Physicochemical Properties Magnesium stearate is supplied as a fine powder with lubrication properties similar to other stearates. Low nitrite grades are packaged and handled to reduce contamination risk and preserve impurity profiles. Procurement choices focus on compatibility with downstream testing and dissolution requirements.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Calcium Stearate is a widely used excipient that serves as a lubricant and flow aid in tablet and granulation processes. It is selected to improve powder flow and reduce die friction during high-speed compression. Typical procurement use includes tablet formulation, direct compression support, and as a glidant in powder blends where controlled release of active ingredients is not affected by lubrication chemistry. Composition & Physicochemical Properties Calcium stearate is a stearate salt used as a hydrophobic lubricant. It is compatible with common tablet excipient systems and is blended at low loadings to achieve ejection and flow benefits. Packaging and handling follow standard industrial excipient practice for powdered materials and are chosen to maintain dry storage conditions for bulk supplies.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Sodium Stearyl Fumarate (SSF) is an excipient lubricant used in tablet formulation to aid ejection and improve surface finish. It is favored where fumarate-based lubrication and sodium counter-ion benefits are sought. Procurement teams use SSF for its predictable blending behaviour and direct compression compatibility. Composition & Physicochemical Properties SSF is supplied as a stable powder compatible with typical blending operations. It is chosen for its lubrication profile and for formulations where alternative stearate chemistries are being evaluated for process or dissolution outcomes. Packaging maintains dryness and ease of handling at production scale.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Stearic Acid is a fatty acid excipient commonly used as a lubricant, emulsifier, and processing aid in tablet and topical formulations. It assists in binding and compression performance and can act as a hydrophobic lubricant in selected systems. Procurement teams source stearic acid for consistent batch-to-batch performance and to support scale-up from R&D to production. Composition & Physicochemical Properties Stearic acid is supplied as a technical-grade fatty acid powder compatible with conventional blending and granulation processes. It is handled and packaged to protect against moisture and to preserve flow characteristics during storage and dosing into process lines. Standard supply formats support production-scale handling.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility Clean Label Lubricant is an excipient targeted at formulators seeking minimal-ingredient or label-friendly tablet lubricants. The material supports tablet ejection and handling while aligning to label preferences valued by nutraceutical and OTC product lines. It is chosen where formulators require lubricant performance with simplified ingredient declarations. Design, Format & Packaging The lubricant is supplied in production-ready powder form compatible with standard blending and compression equipment. Packaging options include lined bags or drums for manufacturing-scale orders. Procurement teams use this material when developing products that prioritize clean label claims without compromising manufacturing efficiency.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Microcrystalline Cellulose (MCC) is a fundamental excipient used as a filler and binder in tablet manufacture and direct compression processes. It provides reliable compressibility and contributes to tablet mechanical strength. Procurement teams specify MCC grades to meet compressibility and dissolution targets during scale-up from development to production. Composition & Physicochemical Properties MCC is supplied as a processed cellulose powder with consistent particle size and flow characteristics to support predictable blending and compression. Packaging preserves dryness and facilitates safe handling at production scale.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Magnesium Stearate is a standard lubricant and flow aid used extensively in tablet and capsule production. It reduces die friction and assists in consistent ejection across different tablet tooling. Procurement teams specify magnesium stearate for reliable blending and compression behaviour across production batches. Composition & Physicochemical Properties Magnesium stearate is supplied as a free-flowing powder intended for blending into powder mixes at low percentages. Packaging and storage preserve the dry state to avoid caking and preserve flow. It is compatible with many common excipients and direct compression systems.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility Lubricant for Effervescent Tablets is an excipient-grade lubricant formulated to improve tablet ejection and surface finish during effervescent tablet compression. It is supplied as an excipient material suited for formulation processes where rapid disintegration and effervescence are required. The material is selected to minimise interference with effervescence chemistry while enabling reliable die release and tablet handling during automated production lines. Design, Format & Packaging The excipient is provided in stable powder form compatible with standard high-shear blending and direct compression lines. Packaging options accommodate drum or bag formats for institutional use and production runs. Typical procurement buyers include formulation teams, QA/QC managers, and production planners at tablet manufacturing sites that require consistent flow and compressibility performance for effervescent product lines.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Mono/Di/Tristearate stearate excipients are supplied as lubricant, anti-adherent, and flow-aid ingredients for tablet manufacturing lines. Choice among sodium, zinc, and aluminium salts affects lubricating efficiency and potential interactions with API and dissolution. Procurement focuses on fatty-acid profile, consistency, and COA availability to ensure manufacturing reproducibility. Technical evaluation considers lubricant concentration and its impact on tablet hardness and disintegration. Composition & Physicochemical Properties Stearate salts are fatty-acid-based lubricants differing by cation. Select the variant that balances lubrication with minimal effect on dissolution; validate compatibility during formulation trials.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Croscarmellose Sodium is supplied as a cross-linked polymer superdisintegrant used widely in tablet manufacture to ensure rapid breakup and API release. Selection requires assessment of swelling and wicking performance relative to tablet hardness and inclusion level. Procurement priorities include consistent functional performance, low microbial load, and COA availability. Technical evaluation should align grade choice with compression parameters and dissolution goals. Composition & Physicochemical Properties Croscarmellose is an anionic cross-linked cellulose derivative designed for rapid hydration and swelling. It is typically used at low concentrations to provide rapid disintegration in aqueous media.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Pregelatinized Starch is supplied as a multifunctional excipient used for binder and disintegrant roles and as an aid for direct compression. Its pregelatinized state imparts improved water uptake and binding without heat treatment during manufacturing. Technical selection focuses on pasting viscosity, particle-size distribution, and compaction behavior to ensure reliable tablet performance. Procurement attention centers on consistent functional performance and lot-level documentation. Composition & Physicochemical Properties Pregelatinized starch combines native starch properties with modified hydration behavior. It offers quick wetting and binding characteristics and is compatible with common tablet excipients.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Ferric Oxide is supplied as an excipient pigment for tablet and capsule coatings and for coloration in finished dosage forms. It is used where inert, stable coloration is required without impacting formulation stability. Procurement priorities include color grade consistency, low heavy-metal content, and compatibility with coating binders and solvents. For coating operations, particle size and dispersibility inform processing and final appearance. Composition & Physicochemical Properties Ferric oxide pigments are inorganic iron oxides with stable color performance. Choose grades based on color depth, particle size, and opacity requirements. Handle per standard pigment safety and dust-control practices in manufacturing.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Sodium Starch Glycolate (SSG) is supplied as a high-performance superdisintegrant for tablet formulations to promote rapid disintegration and consistent dissolution. Selection of grade impacts swelling index, rate of water uptake, and disintegration performance. Procurement focuses on consistent functional performance, low microbial load, and COA availability. Technical evaluation should include swelling index and particle-size distribution to align with target dissolution criteria. Composition & Physicochemical Properties SSG is a cross-linked starch derivative engineered for rapid water uptake and swelling. It is compatible with standard binder systems and commonly used at low inclusion rates to drive disintegration.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Carboxymethyl Cellulose Sodium (CMC-Na) is supplied as a water-soluble polymer excipient used as a viscosity modifier, thickener, and binder in oral and topical formulations. Viscosity grade selection affects suspension stability and mouthfeel in liquid products and matrix strength in solid forms. Procurement focuses on consistent viscosity profile, low microbial load, and lot-level test documentation for QC acceptance. Technical evaluation should reference target viscosity and intended concentration ranges. Composition & Physicochemical Properties CMC-Na is an anionic cellulose derivative with defined viscosity grades. It hydrates rapidly and imparts pseudoplastic behavior in aqueous systems. Assess grade compatibility with other formulation polymers and preservatives.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Purified Talc is supplied as an excipient for glidant, lubricant, and coating filler roles in solid dosage manufacturing. Buyers prioritize controlled particle size, low impurity content, and consistent bulk density to maintain process stability. Technical evaluation includes flowability, lubrication effect during compression, and dispersion in coating systems. Proper packaging is important to avoid contamination and moisture ingress during storage and transit. Composition & Physicochemical Properties Purified talc is a hydrated magnesium silicate mineral processed to remove coarse particles and impurities. Select grades by PSD and bulk density to match blending and coating requirements.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Hypromellose Phthalate is provided as an enteric coating polymer for delayed-release formulations. It is selected where gastric resistance and targeted intestinal release are required. Procurement priorities include consistent substitution grade, film-forming properties, and batch documentation supporting dissolution behavior. Technical assessment focuses on polymer substitution degree, molecular weight distribution, and compatibility with plasticizers and pigments. Composition & Physicochemical Properties Hypromellose Phthalate is a phthalated cellulose derivative designed to resist low pH and enable enteric release. Match grade and formulation to desired disintegration and release profiles during product development.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Simethicone is supplied as an inactive excipient used primarily as an antifoaming and defoaming agent in oral pharmaceutical formulations. It is selected where gas entrapment in suspensions or emulsions may impair product uniformity. For formulation teams, consistent viscosity and droplet size behavior are critical evaluation endpoints. Buyers seeking supply for production batches typically verify COA parameters such as active content and residual solvents where applicable. Packaging options and particle handling recommendations should be matched to manufacturing equipment and scale. Composition & Physicochemical Properties Simethicone is a silicone-based antifoaming agent with low surface tension. It is typically incorporated at low percentage levels to control foaming during production and improve dispensing properties. Compatibility testing with surfactants and emulsifiers is recommended during formulation design. Storage and handling guidance should follow standard excipient practices to retain product performance.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Polyethylene Glycol (PEG) powder is offered as an excipient for formulation roles including binder, plasticizer, and solubilizer across oral and topical products. Selection of molecular-weight grade influences melting point, solubility, and plasticizing effect. Procurement priorities include grade consistency, residual impurity control, and lot-level documentation. Technical teams typically evaluate PEG grade against desired release behavior and processing temperature windows. Composition & Physicochemical Properties PEG powder is a polyether polymer available in multiple molecular-weight grades. It is inert under normal formulation conditions and compatible with a wide range of APIs and excipients; compatibility testing is recommended for new formulations.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Tribasic Calcium Phosphate is supplied as an inorganic filler and diluent for tablet and solid dosage formulations. It provides compressibility and mineral content where formulation design requires calcium-based bulking. Formulation teams evaluate particle size distribution, moisture content, and compressibility to optimize tablet hardness and dissolution. Procurement for production often emphasizes consistent particle distribution to reduce batch variability and maintain manufacturing throughput. Packaging choices and batch documentation support integration into regulated manufacturing lines. Composition & Physicochemical Properties Tribasic Calcium Phosphate is an alkaline calcium phosphate salt used as a diluent. It is typically characterized by controlled particle size and low humidity uptake to preserve flow and tableting performance. Compatibility testing with binders and disintegrants is recommended during formula development.
Min. Order: 1 Unit
GST
Assay Purity & Pharmacopoeial GradeMagnesium Hydroxide and Magnesium Oxide are offered as formulation-grade alkalizing and antacid agents. Buyers evaluate assay purity, loss-on-drying, and particle-size distribution to determine suitability for tablets, suspensions, and powders. Hydration state and reactivity guide selection for specific applications.Composition & Physicochemical PropertiesThese magnesium salts provide alkaline buffering and neutralizing activity. Selection depends on desired neutralizing strength, solubility, and rate of reaction in gastric conditions. Packaging protects powders from moisture and supports safe handling during production.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Dibasic Calcium Phosphate Anhydrous is a commonly used inorganic excipient for oral solid dosage forms serving as a diluent and source of calcium. It supports tablet hardness and compressibility when matched with appropriate binders and lubricants. Quality attributes such as assay, humidity control, and particle-size distribution influence tableting performance, dissolution, and process yield. Buyers focused on production scale prioritize consistent material properties and lot-level documentation to support QC acceptance. Composition & Physicochemical Properties The anhydrous salt form offers reduced moisture uptake compared with hydrated grades and is selected where moisture sensitivity must be minimized. Particle morphology and flow characteristics should be evaluated against the target compression process.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Dibasic Calcium Phosphate Dihydrate is offered as a formulation excipient suited to tablet and solid dosage applications. The dihydrate form affects moisture equilibrium and may be selected where controlled hydration improves tableting behavior. Technical evaluation focuses on particle-size distribution, moisture content, and compressibility characteristics to ensure consistent tablet performance. Procurement for production-scale orders emphasizes specification stability and lot-level QA documentation. Composition & Physicochemical Properties The dihydrate form contains bound water that can influence blend flow and compaction. Match grade selection to process conditions and downstream stability testing to avoid moisture-driven variability.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Aluminium Hydroxide is offered as a pharmaceutical excipient suited for antacid formulations and buffering in oral solid dosage development. It is commonly used to adjust pH, stabilize active ingredients, and provide antacid activity where formulation design requires a basic inorganic excipient. Procurement teams and formulation chemists source this excipient for tablet cores, coating formulations, and suspension buffering roles. Batch traceability and specification checks support integration into existing compounding or production workflows. For institutional buyers the focus is on consistent assay, particle distribution, and low impurity profile to maintain formulation predictability. Composition & Physicochemical Properties Aluminium Hydroxide functions chemically as an inorganic base with buffering capacity. It is typically supplied as a fine particulate suitable for blending with common pharmaceutical excipients. Material handling notes and compatibility with common binders and fillers should be verified in formulation trials. Sourcing options include drum or bulk pack formats for manufacturing environments and sealed packaging for institutional supply chains.
Min. Order: 1 Unit
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Active Compound Concentration & StandardizationFerrous Fumarate is provided with elemental iron assay and impurity profiling to support accurate dosing in supplements and medicinal products. Buyers examine particle-size distribution and stability under intended storage conditions. Selection of this salt depends on desired elemental iron per dose and formulation compatibility.Format, Solubility & StabilityThe salt offers higher elemental iron per unit mass than some alternatives and is used in tablets and capsules. Solubility and potential gastrointestinal tolerability considerations influence formulation choices. Proper packaging reduces exposure to moisture and oxidation.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradeMagaldrate is provided as an active excipient used in antacid formulations. Buyers assess assay purity and standard assay parameters to ensure therapeutic dosing and formulation stability. The compound's acid-neutralizing capacity is a key performance metric in selection.Composition & Physicochemical PropertiesMagaldrate is an aluminium-magnesium hydroxide complex with neutralizing action. Key parameters include neutralizing value per gram, particle-size distribution, and compatibility with other formulation components. Packaging preserves product integrity during storage.
Min. Order: 1 Unit
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Active Compound Concentration & StandardizationFerrous Sulphate is provided with assay and elemental iron content data to support formulation dosing. Buyers review impurity profiles and solubility characteristics to ensure compatibility with final dosage forms. Particle size and flow influence blending and encapsulation performance.Format, Solubility & StabilityThe salt dissolves to release ferrous ions and is used in oral supplement formulations. Stability in finished formulations and potential interactions with excipients are tested in development. Packaging prevents oxidation and moisture exposure during storage.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradeSodium Carbonate is supplied in grades suited for pH control and formulation processing. Buyers verify assay purity and impurity profiles relevant to their application. Physical properties such as bulk density and particle size affect dosing and dissolution behavior.Composition & Physicochemical PropertiesThe material is an alkaline carbonate salt with predictable buffering capacity in aqueous media. Selection criteria include moisture content and compatibility with other formulation ingredients. Packaging options protect against moisture and caking during storage.
Min. Order: 1 Unit
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Active Compound Concentration & StandardizationCalcium Citrate is provided with assay information relevant to formulation dosing and nutritional labeling. Buyers assess elemental calcium content and impurity profiles to ensure blend accuracy. Powder form and particle-size distribution influence blending and encapsulation performance.Format, Solubility & StabilityThe salt offers moderate solubility and stable handling characteristics for nutraceutical and pharmaceutical applications. Selection should consider dissolution behavior and interaction with binders or acidifying agents. Packaging preserves dryness to maintain flow and dosing consistency.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradeSodium Bicarbonate is supplied in grades suitable for pharmaceutical and food-related formulations where buffering or effervescent action is required. Buyers assess assay purity and chloride content when qualifying suppliers. Grade selection influences stability and processing behavior in wet granulation or effervescent tablet production.Composition & Physicochemical PropertiesThe powder is granular and free-flowing where specified; key parameters include particle-size distribution and bulk density. Compatibility with acids, binders, and flavor systems should be checked during formula development. Packaging protects against moisture ingress to preserve functionality.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradeMagnesium Citrate is supplied as an excipient-grade salt for formulation use in supplements and pharmaceutical blends. Buyers evaluate assay purity and residual solvent parameters when qualifying a source. The choice of hydrated versus anhydrous grades impacts dosing and blending behavior.Composition & Physicochemical PropertiesThe material provides soluble magnesium ions with citrate counter-ion, aiding bioavailability in finished products. Key selection factors include solubility, pH effect, and hygroscopicity. Packaging is configured to protect against moisture and ensure flow for dosing equipment.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradeSodium Chloride is provided in grades appropriate for pharmaceutical and laboratory applications where ionic strength and isotonicity are required. Qualification criteria include assay purity, chloride content, and particulate specification. For saline and buffer preparations, consistent assay and low trace impurities are essential.Composition & Physicochemical PropertiesAs a crystalline ionic salt, sodium chloride dissolves readily in water and contributes predictable osmolarity. Selection considers particle size for dissolution rate and equipment dosing behavior. Packaging protects against moisture and contamination during storage and handling.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradeMagnesium Lactate is provided as a formulation-grade magnesium salt favored for its solubility and bioavailability characteristics. Qualification criteria include assay purity and residual solvent content. The hydrated state influences handling and dosing considerations in blends.Composition & Physicochemical PropertiesThe salt delivers magnesium cations complexed with lactate anions and dissolves readily in aqueous media. Particle-size distribution and moisture content are key parameters for encapsulation and tablet production. Packaging preserves dryness and flowability.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradeTitanium Dioxide is offered in grades tailored for pharmaceutical coating and opacifying use. Key buyer checks include particle-size distribution, pigment grade, and impurity profile. Controlled particle size supports uniform coating appearance and process reproducibility.Composition & Physicochemical PropertiesThe pigment is a white, inorganic oxide chosen for opacity and color stability. Surface treatment and milling grade influence dispersion in coating vehicles. Packaging is designed to limit dust generation and preserve pigment integrity during handling.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradeCalcium Carbonate is offered in grades used as a filler, buffering agent, or antacid ingredient in pharmaceutical and nutraceutical products. Buyers evaluate assay and heavy-metal limits when qualifying a supplier. Particle size and surface area influence compressibility and blending performance.Composition & Physicochemical PropertiesThe material is a stable inorganic carbonate with typical granular or powdered forms depending on processing. Important selection factors include particle-size distribution, bulk density, and residual moisture. Proper packaging prevents contamination and moisture ingress.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradePotassium Sulphate is presented as a formulation-grade inorganic salt used where chloride-free potassium is needed. Procurement focuses on assay purity and sulfate content to ensure compatibility with finished-product specifications. The compound's solubility and ionic strength are key parameters in formulation design.Composition & Physicochemical PropertiesThe material provides sulfate anions with potassium cations and is typically delivered as a crystalline salt. Particle size and bulk density affect handling and dosing in mixer systems. Packaging is chosen to limit moisture uptake during storage and transit.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradeMagnesium Sulphate is offered in grades for pharmaceutical, laboratory, and industrial uses where a soluble magnesium source is required. Buyers check assay purity, sulfate content, and particulate limits during supplier qualification. Hydration state affects dosing and storage conditions.Composition & Physicochemical PropertiesThe salt dissolves readily and provides magnesium ions for formulation or reagent purposes. Particle-size distribution and bulk density affect flow and dosing accuracy. Packaging protects against moisture to preserve the salt's functional characteristics.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility This Safety IV Cannula Without Port And Wings uses a passive telescopic safety mechanism and covers sizes 14â24G. The telescopic design provides a compact shielding action and is typically selected where minimal handling and compact device form are priorities. Sterile single-use packaging is standard and buyers evaluate activation ergonomics and compatibility with disposal routines before placing institutional orders. Gauge range includes larger bore options for higher-flow requirements. Design, Format & Packaging The telescopic safety profile allows a low-profile device suited for constrained insertion sites. Packaging is single-unit sterile pouches organized into cartons for ward supply. Buyers should confirm carton counts to match usage patterns and restock schedules.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility The IV Cannula With Small Wings And Wing-Holder combines small fixation wings with an integrated holder to improve securement at the insertion site. The device is supplied sterile for single use; procurement focuses on wing dimensions, fixation compatibility with dressing materials, and carton-pack options. Small wings help streamline dressing while the wing-holder eases handling during insertion and tape application. Design, Format & Packaging Packaged as sterile single units in cartons, the wing-holder design supports straightforward bedside fixation. Institutional buyers choose carton sizes that match ward consumption patterns to simplify restock and inventory turnover.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility The Large Animal Veterinary Catheter is intended for clinical use in veterinary hospitals and field surgical units. Product titles do not specify material composition; buyers typically select catheters based on diameter, length, and sterility class for species-specific applications. Veterinary procurement emphasizes robust packaging and sterility for field deployment and operating-suite procedures. Communicate expected animal species and clinical use when requesting specifications to ensure correct dimensioning. Design, Format & Packaging Design variants for large-animal catheters address strength and handling in field conditions; packaging options often include multiple sterile pouches per carton to support mobile clinics. Specify required dimensions and pack-counts to align supply with clinical and surgical schedules.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility The Pen Type IV Cannula without wings offers a compact insertion profile suitable for settings where low-profile devices are preferred. The product is provided sterile and for single use; buyers select gauges based on flow needs and dressing preferences. Pen-type models reduce bulk at the insertion site and are often chosen for pediatric care and outpatient procedures where minimal obstruction is desired. Design, Format & Packaging Pen type cannulas are packaged individually in sterile pouches and grouped into cartons suitable for clinic restock. Buyers typically specify carton sizes to match clinic reorder cycles and minimize on-site storage footprint.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility The IV Cannula Without Wings provides a compact option for peripheral venous access where wings are not desired. The device is supplied sterile for single-use clinical insertion and buyers typically select gauges by intended infusion flow and patient profile. Wingless designs are common in neonatal, pediatric, or placement-constrained applications where a low profile assists patient comfort and dressing adhesion. Design, Format & Packaging Packaged as single sterile units within hospital cartons, wingless cannulas are offered in multiple gauges. Institutional procurement often standardizes carton sizes to match ward demand and minimize storage requirements.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility The IV Cannula With Port And Wings is configured for stable fixation and direct IV set connection through an integrated port. Supplied sterile for single use, it supports routine infusion therapy and secure tubing connection in wards and infusion centers. Buyers prioritize port compatibility with existing IV sets and easy dressing fixation to reduce dislodgement events. Design, Format & Packaging Ported, winged cannulas are supplied as single sterile units in cartons sized to hospital requirements. Specify preferred pack-count and port compatibility when requesting procurement quotes.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility The Decompression Needle is a single-use clinical needle intended for emergency decompression procedures. The title does not specify gauge or length; procurement teams select a needle based on intended anatomical application and clinical protocol. Sterile, individually sealed packaging is standard for emergency devices to allow immediate deployment. Confirm required length and gauge when requesting a catalog quote to ensure clinical applicability. Design, Format & Packaging Design focuses on rapid deployment and clear activation; packaging aligns to emergency kit inclusion and may be specified in single-unit or multi-unit cartons depending on procurement need. Buyers typically coordinate pack-counts with kit assembly requirements.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility The IV Cannula With Small Wings offers a balance between secure fixation and a lower profile for patient comfort. The device is supplied sterile for single use; gauge and wing dimension selection is a procurement detail typically confirmed by the clinical team. Small wings are commonly specified for pediatric or ambulatory settings where bulkier wings are undesirable. Design, Format & Packaging Packaged individually for sterility and bundled into cartons, the small-wings design supports quick fixation and simple dressing. Buyers select carton sizes to meet clinic throughput and restock cadence.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial GradeZinc Sulphate is offered as a formulation-grade inorganic salt commonly used in pharmaceutical and nutraceutical formulations. It supports mineral supplementation blends and acts as a source of zinc in compound formulations. Procurement teams evaluate assay purity, heavy-metal limits, and COA traceability when selecting a zinc salt for production batches.Composition & Physicochemical PropertiesThe material is anhydrous or hydrated zinc sulphate salt with soluble ionic behavior in aqueous systems. Typical selection criteria include solubility profile, pH impact in solutions, and compatibility with binders and fillers. Packaging formats vary by order size to support drum, bag, or packed container requirements for manufacturing lines.
Min. Order: 1 Unit
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Assay Purity & Pharmacopoeial Grade Zinc Chloride is listed as an excipient-grade chemical commonly used in formulation and industrial processes. The raw product title does not state an assay or pharmacopoeial grade; buyers typically request assay purity, moisture limits, and relevant test methods when specifying Zinc Chloride for formulation. For procurement, specify required assay and any compendial grade to ensure the supplier provides the correct material and documentation. Composition & Physicochemical Properties Zinc Chloride as an inorganic salt is selected for its ionic and solubility properties in formulation tasks. Packaging and handling considerationsâdrums, lined containers, or smaller packsâare important for storage and dosing accuracy in formulation lines. State desired pack-size and quality parameters in RFQs to receive accurate offers.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility The Safety IV Cannula Without Port And Wings in this listing features an active spring-activated safety mechanism and covers sizes 14â26G. Active safety engages automatically via an internal spring and is selected where automatic shielding is preferred to reduce handling steps at removal. Buyers focus on activation reliability, single-use sterile packaging, and compatibility with disposal practices in hospitals and surgical theatres. Gauge coverage includes larger diameters for higher-flow needs as well as smaller diameters for routine peripheral access. Design, Format & Packaging Without wings or a port, the device is compact and packaged individually for sterile storage. Hospital procurement commonly requests carton pack-counts aligned to procedure suites and perioperative kits. Specify required gauge range and pack counts for tailored quotations.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility The Closed System IV Cannula is designed for safe peripheral access and reduces fluid contamination risk by maintaining a closed pathway during use. The product title explicitly lists sizes 18â24G; these gauge options support a range of flow and therapy needs in clinical settings. Buyers prioritize sterility assurance and single-use packaging for infection control in hospital and outpatient infusion units. Confirm gauge and packaging preferences when planning procurement to align with clinical protocols. Design, Format & Packaging Closed-system design supports reduced fluid exposure and is supplied in sterile, individually sealed pouches suitable for hospital inventory. Packaging options help maintain aseptic handling during storage and at the bedside. Institutional buyers commonly select carton pack-counts that match ward turnaround and inventory replenishment cycles.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility This Safety IV Cannula Without Port And Wings includes a passive safety mechanism housed in a plastic case to lock or shield the needle after use. The title lists sizes 18â24G, indicating broad gauge coverage for many institutional infusion tasks. Single-use sterile supply is implied by the device class; procurement teams focus on consistent sterile packaging and handling for hospital safety programs. Buyers also evaluate ease-of-activation and compatibility with existing bedside workflows. Design, Format & Packaging The cannula omits a port and wings to support compact placements and is packaged individually to preserve sterility. Plastic-case passive safety reduces post-use exposure risk and suits standard disposal protocols. Hospital buyers often standardize on a single pack-count to simplify inventory and minimize on-ward handling complexity.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility Midline IV Cannula with Safety Feature is engineered for reliable peripheral venous access in institutional care. The product title indicates an integrated safety mechanism designed to reduce needlestick risk during and after insertion. This device is intended for single-use clinical workflows and for teams that require a predictable device profile across ward and infusion therapy programs. Procurement teams and clinical engineers evaluate these midline devices primarily by gauge availability, safety activation type, and packaging configuration. Design, Format & Packaging The cannula is supplied in sterile, single-unit packaging designed for aseptic tray use. Packaging supports hospital inventory systems and aims to simplify bedside deployment during IV therapy or intermediate vascular access. For ordering, buyers typically confirm gauge, safety style, and preferred packing count to align with ward usage patterns and restock cadence.
Min. Order: 1 Unit
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Material, Biocompatibility & Sterility Safety IV Cannula With Port And Wings includes a port for secure IV connection and wings for fixation to the skin. The passive safety mechanism is housed in a plastic case to shield the needle after use and lower needlestick risk. The title lists sizes 18â24G which supports a wide clinical range from medium to lower flow rates. Institutional buyers prioritize sterile single-use packaging and ease of fixation in busy ward environments. Design, Format & Packaging The winged design simplifies dressing and tape fixation. Packaging is oriented toward sterile single-unit pouches and hospital cartons suitable for inventory management. Buyers typically specify preferred pack-count per carton and any special labeling or batch documentation needs at quoting time.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility This safety IV cannula features a metal-clip passive safety mechanism in a winged, ported format sized 18â24G. The metal-clip mechanism provides an alternative activation and locking profile compared with plastic-case designs and may be preferred based on clinical handling preferences. Buyers focus on sterility, single-use packaging, and the activation profile of the metal clip during acceptance testing. Gauge coverage supports a wide range of infusion therapy needs across hospital departments. Design, Format & Packaging The winged and ported hub design supports stable fixation and quick connection to IV tubing; sterile, single-unit pouches are standard. Hospital procurement commonly requests carton pack-counts to align with ward inventory cycles and to streamline reordering.
Min. Order: 1 Unit
GST
Double-Lumen Central Venous Catheter. Offered in 4 Fr to 8 Fr sizes with multiple length options. The two-lumen design enables concurrent infusion and monitoring tasks while minimizing line cross-contamination. This variant suits clinical environments that require dual-access capability with flexible sizing.
Min. Order: 1 Unit
GST
Safety Blood Collection Needle With Holder. This preassembled needle-and-holder kit provides a safety-engineered option for venous blood collection and routine phlebotomy. The integrated safety mechanism reduces sharps exposure during use and disposal. It is appropriate for diagnostic laboratories, outpatient clinics, and hospital phlebotomy stations that require packaged collection assemblies.
Min. Order: 1 Unit
GST
Single-Lumen Central Venous Catheter. Available in 14 Ga through 22 Ga gauges and lengths of 15, 16 and 20 cm. This single-lumen option is appropriate when a single dedicated channel is required for therapy or sampling. Selection should match intended infusion rates and clinical workflow needs.
Min. Order: 1 Unit
GST
Safety Blood Collection Needle Without Holder. This safety needle is supplied as the sterile needle component for facilities that use existing holders or custom assembly workflows. The integrated safety feature reduces sharps risk during withdrawal and disposal. Procurement of needle-only SKUs supports inventory flexibility for diagnostic labs and large clinical programs.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility P-Lyne 1.9 Fr x 40 cm Neonatal PICC Line Catheter is sized for neonatal venous access where a narrow French size and appropriate length are essential. The 1.9 Fr diameter supports safe infusion and sampling in neonates while the 40 cm length is chosen to permit central placement from peripheral access points typical in neonatal care. Design, Format & Packaging The catheter is provided as a sterile single-use device including insertion accessories and securement aids. Packaging aligns with neonatal unit requirements, and procurement options include sterile trays or pouches tailored to clinical workflow.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility Arterial Catheter Kit 20G 3x8 cm PU offers a fine-gauge option suitable for low-flow sampling and pediatric or small-vessel arterial access. The 20G gauge and compact 3x8 cm length support procedures where reduced insertion profile and shorter external length are preferred. Polyurethane construction typically balances flexibility and handling for short-term arterial monitoring. Design, Format & Packaging Kits are provided as single-procedure sterile assemblies and can be packaged to align with pediatric care unit stocking and operating-room requirements. Procurement options include sterile pouches and tray formats to suit clinical workflows.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility P-Lyne 4 Fr x 60 cm Power Injector-CT PICC Line Catheter offers injector-rated capability in a narrower French size. The 4 Fr lumen is chosen where injector compatibility is required alongside a preference for a smaller catheter diameter. The 60 cm length supports central tip placement appropriate to imaging and interventional workflows. Design, Format & Packaging Catheters are supplied sterile with insertion accessories and can be packaged to meet radiology department inventory and sterile-field requirements. Procurement may specify pack-count and documentation needs when requesting a quote.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility P-Lyne 6 Fr x 60 cm Power Injector-CT PICC Line Catheter is engineered for power-injectable contrast administration during CT and interventional imaging. The 6 Fr diameter supports injection flow rates required for powered contrast delivery while the 60 cm length supports central positioning. Procurement for radiology units focuses on injector compatibility and catheter construction that supports rated pressures and imaging workflows. Design, Format & Packaging The device is supplied sterile and configured for single-use insertion with accessories. Packaging formats can be aligned with radiology department stocking and sterile-field needs.
Min. Order: 1 Unit
GST
PICC Line Catheter 5 Fr x 60 cm Standard. This peripheral inserted central catheter is sized for central venous access with a 5 Fr lumen and 60 cm length. It suits infusion therapy, long-term antibiotic administration, and vascular access management in hospitals and infusion centers. The catheter is intended for institutional procurement, inventory planning, and clinical deployment where a mid-range French size is required.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility P-Lyne 6 Fr x 60 cm Standard PICC Line Catheter is specified for prolonged central venous access where a larger lumen supports infusion therapy, parenteral nutrition, and frequent sampling. The 6 Fr size and 60 cm length are selected for central tip placement with consideration for therapy type and patient anatomy. Design, Format & Packaging Supplied as a sterile single-use device with insertion accessories, the standard PICC configuration supports clinical and home-infusion programs. Packaging and pack-counts can be tailored to procurement needs.
Min. Order: 1 Unit
GST
PICC Line Catheter 5 Fr x 60 cm Power Injector Compatible. This 5 Fr catheter is manufactured and rated for power injection during CT imaging, enabling contrast administration through the same central access. It combines vascular access for continuous infusion with confirmed compatibility for image-guided contrast injection. Ideal for hospitals and imaging departments that require integrated vascular access for therapy and diagnostic imaging.
Min. Order: 1 Unit
GST
PICC Line Catheter 4 Fr x 60 cm Standard. The 4 Fr size provides a lower-profile central access option for therapies requiring smaller lumen diameters while maintaining central placement. At 60 cm length it supports placement into central venous targets for extended infusion or intermittent therapy. This variant is appropriate for facilities managing pediatric-to-adult venous access where a slimmer catheter profile is preferred.
Min. Order: 1 Unit
GST
PICC Line Catheter 3 Fr x 60 cm Standard. The 3 Fr variant is a low-profile central catheter option designed for clinical situations requiring a smaller lumen, including select pediatric and fragile-vein scenarios. At 60 cm it supports central tip placement and is intended for controlled infusion regimens. Procurement teams use this SKU when device profile and vessel preservation are priority selection criteria.
Min. Order: 1 Unit
GST
Triple-Lumen Central Venous Catheter. Available in multiple French sizes (4.5 Fr, 5.5 Fr, 7 Fr, 8.5 Fr) and lengths (13 cm, 15 cm, 16 cm, 20 cm). The triple-lumen configuration supports simultaneous lines for medication, fluid therapy, and monitoring. These variants address multi-access clinical scenarios in intensive care and high-acuity departments.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility Arterial Catheter Kit 16G 5x11 cm PU is a compact arterial access kit tailored for sites where a shorter catheter length is clinically preferred. The 16G caliber supports routine sampling while the PU construction balances flexibility and kink resistance for short peripheral arterial placements. Design, Format & Packaging Kits may be supplied in sterile single-use pouches or tray formats to match operating-room and ICU stocking. Procurement options include configured pack sizes to streamline clinical replenishment.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe combi Luer lock connector is manufactured from medical-grade, latex-free polymer and designed for male-female coupling in ISO 80369-7 systems. Connector geometry supports low-dead-space coupling to reduce residual fluid volume. Materials are selected to be compatible with common infusion fluids and to reduce adsorption effects. Each connector is supplied sterile and individually sealed to support aseptic assembly at point of care.Design, Format & PackagingThe combined male-female Luer lock enables secure connections between devices and administration sets while meeting ISO 80369-7 dimensional compatibility. The design reduces accidental disconnection and simplifies secure coupling in clinical workflows. Units are individually pouch-packed and boxed for central supply distribution with lot and expiry labelling for inventory control.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility Arterial Catheter Kit 16G 5x20 cm PU is designed for invasive arterial access and continuous hemodynamic monitoring. The kit's 16G gauge and 5x20 cm length indicate the lumen size and catheter length used for arterial line placement in ICU and surgical settings. The PU notation indicates a polyurethane catheter construction commonly chosen for flexibility and vessel wall conformity in arterial access applications. Design, Format & Packaging The kit typically includes the arterial catheter, insertion needle, guidewire, and connection tubing arranged for single-procedure use. Packaging options can be tailored to sterile single-use trays or bulk sterile pouches to match hospital inventory protocols and operating-room replenishment needs.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe latex-free heparin cap is fabricated from medical-grade, transparent polymer compatible with ISO 80369-7 connector standards. The latex-free construction reduces allergen exposure and supports broad clinical deployment. The cap design includes a heparin-compatible septum to assist intermittent flush and access protocols. Each cap is supplied sterile to support aseptic handling during line maintenance.Design, Format & PackagingThe transparent cap allows visual inspection of line content and flashback during access. Designed for ISO 80369-7 compatibility, connectors fit standard low-dead-space luer interfaces. Units are individually sealed in sterile pouches and bulk-packed into cartons for hospital inventory, with lot and expiry marks for QA tracking and inventory rotation.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility Luer Cap Standard Taper ISO 80369-7 is designed to meet standard connector dimensions used in contemporary medical device assemblies. The standard taper profile supports broad compatibility across male Luer fittings specified to ISO 80369-7 and reduces the risk of cross-connection by conforming to established connector interfaces. Clinical procurement teams prioritize ISO-conformance where device interoperability and regulatory alignment are required. Design, Format & Packaging The cap features a full-length taper that ensures a reliable seal on compliant connectors and is offered in packaging formats suitable for clinical sterile supply chains. Packs can be configured to match inventory and surgery-suite replenishment workflows, enabling straightforward integration into device assembly or IV set kits.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility Arterial Catheter Kit 18G 4x10 cm PU provides a finer gauge option for arterial access where a smaller lumen is desired. The 18G size balances access with reduced vessel trauma for certain clinical indications. The PU construction offers flexibility and patient comfort during arterial monitoring periods. Design, Format & Packaging The kit is configured for single-procedure use and can be packed in sterile pouches or trays based on procurement preference. Pack-counts and sterile presentation can be aligned to hospital inventory routines.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe latex-free yellow heparin cap uses medical-grade polymer and elastomer components compatible with ISO 80369-7 connectors. The yellow colour denotes a specific line or protocol per institutional colour-coding practices. The cap is latex-free to reduce allergen exposure and is supplied sterile for immediate clinical use. Materials are selected to avoid interaction with heparin flush solutions and to permit clear visual inspection.Design, Format & PackagingThe cap offers a transparent window area for visual assessment and a coloured housing for protocol identification. Luer-compatible connectors ensure compatibility with standard infusion systems. Each unit is individually sealed in a sterile pouch and boxed for hospital stocking, with lot and expiry details printed for QA and inventory control.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility Arterial Catheter Kit 16G 5x15 cm PU is specified for arterial access where a slightly shorter catheter length is preferred, such as radial artery placements. The 16G gauge supports routine sampling and monitoring while the polyurethane construction provides flexibility and vessel conformity appropriate for percutaneous arterial lines. Design, Format & Packaging Kits are arranged for single-procedure use and may include insertion accessories and securement components. Packaging can be specified to match sterile-tray workflows or bulk pouching for inventory stocking.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility P-Lyne 2.0 Fr x 50 cm Paediatric PICC Line Catheter is sized for pediatric and neonatal venous access where a narrow French size and extended catheter length are required. The 2.0 Fr diameter supports infusion and sampling needs for small patients while the 50 cm length accommodates central placement from peripheral insertion sites. Clinical procurement teams consider French size and length when selecting PICC lines for pediatric wards and neonatal intensive care. Design, Format & Packaging The catheter is supplied as a sterile single-use device with insertion accessories and securement components as configured in the kit. Packaging choices support sterile-tray presentation or pouch formats aligned to hospital inventory and insertion protocols.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe disinfecting cap contains a pre-saturated 70% isopropyl alcohol (IPA) medium within a single-use cap housing designed to fit standard needle-free connectors. The IPA concentration is selected to provide rapid surface disinfection while being compatible with common connector materials. Housing materials are medical-grade and latex-free. Each cap is individually sealed to maintain reagent integrity until first use.Design, Format & PackagingThe cap is engineered for straightforward application to Luer-compatible needle-free sites and features a closure that maintains contact between the IPA pad and the connector surface. Caps are supplied in sterile-ready packaging and boxed for institutional stocking. Labels include lot and expiry information to support inventory control and QA checks upon receipt.
Min. Order: 1 Unit
GST
Material, Biocompatibility & Sterility Luer Cap Short Taper provides a compact, secure closure for male Luer fittings used across clinical, laboratory and point-of-care assemblies. The short taper design reduces dead space at the connection and simplifies cap removal during clinical workflows. Intended for single-use clinical procedures, this cap is compatible with standard male Luer connectors and is commonly used to protect catheter ports and infusion lines during handling and storage. Design, Format & Packaging The cap offers a push-fit closure with a short tapered profile to fit tight connector tolerances. It is supplied in sterile-ready packaging formats when required by procurement specifications. Packaging options can be aligned with institutional procurement needs to facilitate inventory control and aseptic handling at point of care.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe one-lumen extension tubing set is manufactured from latex-free medical polymer and supplied sterile for single-use infusion tasks. The negative-displacement valve produces a controlled fluid displacement on access and is compatible with standard Luer fittings. Material selection supports clinical biocompatibility and reduces allergen exposure risks. Units are presented in peelable sterile pouches for aseptic handling during device deployment.Design, Format & PackagingThe 15 cm one-lumen format is compact and intended for simple infusion lines or sampling setups requiring a single dedicated channel. Luer-compatible connectors allow direct integration with infusion pumps and administration sets. Packaging provides sterile integrity and includes lot identifiers to assist hospital inventory processes. Carton sizes are optimised for clinical stocking and pharmacy distribution.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe two-lumen extension tubing set is composed of medical-grade, latex-free polymer designed for single-use infusion applications. Two separate lumens permit independent medication lines while minimising cross-contamination. Each lumen is sized and colour-marked for easy bedside identification. The needle-less neutral-displacement injection valve supports intermittent syringe access with reduced fluid pushback into the line. Materials are selected to meet standard clinical biocompatibility expectations and to minimise allergen exposure.Design, Format & PackagingThe set measures 15 cm overall and includes two Luer-compatible connectors for direct integration with existing infusion systems. The neutral-displacement valve reduces fluid loss during access and simplifies line management for nursing staff. The compact design lowers line clutter and improves bedspace ergonomics. Each unit is supplied in an individual sterile pouch and bulk-packed in cartons sized for hospital inventory storage.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe three-lumen extension tubing set uses latex-free medical polymers engineered for single-use infusion. The negative-displacement needle-less valve is designed to minimize contamination risk while providing a small positive fluid displacement on access that can help clear the septum. Lumens are independently colour-coded and sized for parallel therapy without cross-flow. Materials align with standard clinical compatibility expectations and the product is supplied sterile for immediate clinical use.Design, Format & PackagingThe 15 cm set features three discrete channels and Luer-compatible connectors for pump and syringe interfaces. The negative-displacement mechanism differs from neutral-displacement valves by producing a controlled displacement that some clinicians prefer for line clearing during injections. Each unit is sealed in a sterile pouch and packed into cartons configured for hospital inventory management. Labelling includes lot and expiry information for receiving checks.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe one-lumen extension tubing set uses medical-grade polymer tubing that is latex-free and intended for single-use infusion tasks. The neutral-displacement needle-less valve lowers fluid backflow during syringe access and is compatible with standard Luer connectors. Material selection emphasizes biocompatibility and minimises allergenic risk in clinical settings. Each set is produced and packaged to support sterile handling at point of care.Design, Format & PackagingThe single-lumen format provides a compact option for straightforward IV therapy or monitoring lines where one access channel suffices. The 15 cm tubing length is convenient for bedside management and reduces excess line length. Connectors are standardized for compatibility with common infusion pumps and sampling accessories. Units are individually sealed in sterile pouches and boxed for institutional distribution.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityHigh-pressure monitoring lines use reinforced medical-grade polymer tubing sized 1.2x2.8 mm to support reliable arterial waveform transmission. Reinforcement and wall thickness are selected to withstand higher transducer pressures while preserving signal fidelity. Connectors match industry-standard transducer fittings and materials are latex-free to reduce patient allergen risk. Each set is supplied sterile for immediate clinical use.Design, Format & PackagingThe tubing assembly includes reinforced sections and secure connectors to resist kinking and to maintain consistent pressure response. Clear tubing sections allow visual inspection of fluid continuity and air bubble management. Units are individually pouch-packed and boxed for central supply, with lot and expiry labelling to support inventory control and QA inspection upon receipt.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe two-lumen extension tubing set is constructed from latex-free medical polymer suitable for single-use infusion routines. The negative-displacement needle-less valve offers controlled displacement on access to manage line patency. Each lumen is colour-coded for rapid clinical identification and sized for common infusion and sampling tasks. The materials used support standard clinical biocompatibility expectations and the unit is supplied sterile in tamper-evident pouches.Design, Format & PackagingThe 15 cm tubing length balances bedside flexibility with minimised excess line. Luer-compatible connectors ensure compatibility with pumps and injection devices. The negative-displacement mechanism assists some clinical workflows by clearing septum material during injection. Each set is individually pouch-packed and boxed into cartons configured for pharmacy and central supply storage.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe RightSpot pH indicator vial is formulated to provide a rapid bedside pH check for enteral tube placement verification. The indicator chemistry responds across the gastric to respiratory pH range, allowing clinical staff to assess placement through aspirate sampling. The vial design supports single-use testing and is packaged to maintain reagent integrity until first use. Materials in contact with samples are chosen to avoid interference with pH response.Design, Format & PackagingThe vial format is compact for point-of-care use and includes a clear reagent window for visual pH comparison. Labels indicate pH thresholds and handling guidance for clinical staff. Each vial is individually sealed and packed in cartons for pharmacy or ward stock. Packaging includes lot identifiers to support inventory control and receiving inspection.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe negative-displacement injection stopper is built from medical-grade elastomer and polymer housing engineered for single-use clinical access. The negative-displacement valve design produces a small inward fluid movement on access that some workflows use to reduce outward leakage. Materials are latex-free to mitigate allergy risk in clinical populations. Units are supplied sterile to maintain aseptic integration into infusion lines.Design, Format & PackagingThe device features a low-profile, Luer-compatible needle-free access port designed for reliable syringe engagement. The negative-displacement action can assist specific line-clearance techniques preferred by some clinicians. Each stopper is individually pouch-sealed and boxed for hospital distribution, with lot and expiry details for inventory management.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityLow-pressure monitoring lines are fabricated from flexible, medical-grade polymer tubing compatible with arterial and venous pressure transducers. The 3.0x4.1 mm tube size provides a lumen profile suited to low-pressure signal fidelity while maintaining structural flexibility for bedside routing. Connectors are Luer-compatible and materials are selected to minimise adsorption and signal dampening. Units are provided sterile to support direct use in monitoring circuits.Design, Format & PackagingThe monitoring line assembly includes standard transducer connectors and a clear tubing section for visual inspection of fluid continuity. Lengths and connectors are configured for bedside monitoring setups and to integrate with common haemodynamic monitors. Each set is sealed in sterile packaging and boxed for central supply distribution, with lot and expiry information included on labels for inventory control.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThis neutral-displacement injection stopper is made from medical-grade elastomer and polymer housings designed for single-use needle-free access. The neutral-displacement mechanism balances fluid movement during access to reduce backflow risks. Materials are latex-free and selected for clinical compatibility with common IV line systems. Each stopper is supplied sterile to maintain aseptic integrity when integrated into infusion lines.Design, Format & PackagingThe device features a low-profile needle-free port compatible with standard Luer connectors and is designed for ease of syringe access. The neutral-displacement action helps preserve line volume during intermittent injections. Each unit is individually sealed and packed into cartons for hospital inventory, with lot marking for QA traceability and stock rotation control.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThis flow regulator infusion set features a vented drip chamber calibrated at 60 drops/mL, a double-scale dial flow regulator, latex-free Y-site, C-clamp, and a male luer lock with cap. Tubing is DEHP-free PVC with a 1700 mm length to support common infusion set-ups. The assembly is intended for single-use sterile supply for IV therapy.Design, Format & PackagingOptional 20 drops/mL drip chamber variants are available as configured SKUs. Each set is packaged sterile and individually sealed to support aseptic handling. Packaging is optimized for clinical storerooms and ward distribution.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe three-lumen extension tubing set is manufactured from medical-grade, latex-free polymer tubing designed for single-use clinical infusion lines. The inner lumens are colour-coded for channel identification and sized to support simultaneous administration and sampling without cross-flow. The needle-less neutral-displacement injection valve reduces fluid backflow risk during intermittent access. Materials are selected to meet common biocompatibility expectations for infusion sets and to avoid latex exposure in sensitive patients. Packaging supports sterile single-pouch presentation for aseptic handling at point of use.Design, Format & PackagingThe set has a 15 cm overall tubing length measured from catheter hub to distal connector and includes three separate lumens for parallel therapy lines. Connectors are Luer-compatible and the valve is a neutral-displacement, needle-free type to minimise fluid loss during injection. The compact design reduces line clutter at bedside while permitting clear labelling and channel management. Each set is individually sealed in a peelable sterile pouch and packed into transit cartons sized for institutional stocking.
Min. Order: 1 Unit
GST
Strength, Dosage Form & Pack ConfigurationHealFlush pre-filled saline flush syringe is supplied as an externally sterile 3 mL unit, gamma-sterilized and ready for use in IV line maintenance and flushing procedures. Each syringe contains a sterile saline solution contained in a pre-filled syringe body with a luer-lock compatible tip to fit common IV line connectors. Packaging options include hospital-ready cartons with lot identifiers for inventory control.Dosage-Form-Specific Handling & Administration ContextSyringes are single-use and intended for flushing catheters and IV lines as part of routine clinical protocols. Handle according to facility aseptic practices and dispose of as clinical sharps waste per local regulations. Provide order details to confirm pack count and delivery timeline for larger institutional requirements.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThis flow regulator extension set includes a female luer lock with cap, double-scale dial flow regulator, latex-free Y-site, male luer lock with cap, and DEHP-free PVC tubing at 450 mm length. The extension is intended for single-use sterile supply and supports common infusion line extensions in clinical settings. The shorter tubing length suits bedside and portable infusion arrangements.Design, Format & PackagingUnits are individually sterile-sealed and packed in cartons with lot-level traceability. The design reduces connector bulk and supports nursing workflows in infusion management.
Min. Order: 1 Unit
GST
Strength, Dosage Form & Pack ConfigurationHealFlush 10 mL pre-filled saline flush syringe is supplied externally sterile and gamma-sterilized for clinical flushing use. The larger 10 mL volume is suitable for protocols requiring higher flush volumes and for use in surgical or infusion settings. Syringes are single-use with luer-compatible tips and are packaged in cartons with lot-level details for inventory control.Dosage-Form-Specific Handling & Administration ContextThese syringes are intended for single-use flushing and should be handled per clinical aseptic guidelines. Disposal must follow local sharps handling protocols. For bulk procurement, indicate packaging and documentation requirements in the RFQ.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe lipid-resistant three-way stop cock features a 45-degree click mechanism and color-coded pegs (red/blue) to assist line identification. Materials are selected to reduce lipid adherence and maintain flow integrity during lipid-based infusions. Each unit is supplied sterile and intended for single-use clinical applications.Design, Format & PackagingThe 45-degree click provides tactile feedback for position selection and reduces accidental rotation. Color-coded pegs simplify staff training and line identification. Packaging supports hospital stocking with lot traceability.
Min. Order: 1 Unit
GST
Strength, Dosage Form & Pack ConfigurationHealFlush pre-filled saline flush syringe is supplied as a 5 mL externally sterile, gamma-sterilized unit for clinical flushing applications. The pre-filled format reduces bedside preparation and supports consistent saline volume for flushing protocols. Syringes include a luer-compatible tip and are packed in cartons with lot identifiers to assist hospital inventory control.Dosage-Form-Specific Handling & Administration ContextIntended for single-use IV flush applications. Follow facility aseptic procedures for handling and dispose of used syringes per sharps waste guidelines. Indicate pack count needs when requesting pricing to confirm MOQ and lead times.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThis lipid-resistant three-way stop cock is designed for use with lipid-containing infusions and parenteral nutrition lines. The stop cock includes extension tubing and a male luer lock with cap. Materials are selected to resist lipid adherence and preserve flow characteristics during infusion sessions. Units are supplied sterile and intended for single use in clinical environments.Design, Format & PackagingManufactured to align with infusion therapy workflows, the product ships in sterile individual pouches and cartons labeled for inventory control. The extension tubing option facilitates placement and access in ICU and infusion settings.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThe lipid-resistant three-way stop cock with 45-degree click action is designed to support lipid infusion workflows. Materials are selected to reduce lipid adherence and ensure consistent flow during prolonged infusions. Supplied sterile for single use, the stop cock meets common clinical handling expectations for infusion accessories.Design, Format & PackagingThe click-action mechanism facilitates precise valve positioning. Packaging is designed for hospital inventories with individual sterile pouches and carton-level lot marking.
Min. Order: 1 Unit
GST
Material, Biocompatibility & SterilityThis adult CO2 sampling nasal cannula is configured with a male luer connector and 2.1 m tubing length for flexible patient monitoring. Manufactured from medical-grade, latex-free polymer, it is supplied sterile and packaged individually. The male luer connection simplifies direct sampling line attachment in clinical monitoring systems.Design, Format & PackagingAvailable as single-use sealed units, the product is packed in cartons with lot identifiers to support hospital inventory control. Ordering options include mixed or uniform connector packs depending on procurement needs.
Min. Order: 1 Unit
GST
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