R K D Pharmaceutical LLP is a globally focused pharmaceutical export and healthcare sourcing company providing access to high-quality pharmaceutical formulations, APIs, excipients, nutraceuticals, medical devices, surgical consumables, laboratory ins...
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Dialysis Consumables
Blood Tubing Set (Pre-Pump, Post-Pump, Premium)
Membrane, Flux Class & Surface Area
Blood Tubing Set (Pre-Pump, Post-Pump, Premium) is a complete single-use bloodline assembly used to connect patient vascular access, pump, dialyzer, and return circuit during dialysis. The premium designation typically indicates enhanced tubing materials or integrated features to improve handling and reduce kinking. Clinical buyers evaluate tubing compatibility with their machines, pump heads, and dialyzer ports to ensure leak-free connections and consistent blood flow during treatment.
Compatibility & Consumable Dependency
These tubing sets are built to interface with standard dialysis machine connectors and dialyzer ports. They are part of the session consumable set including needles, dialyzers, and clamps. Procurement teams must verify pump head compatibility, connector type, and any integrated sensor or port features when placing orders to avoid mismatched assemblies.
High Flux Dialyzer
Membrane, Flux Class & Surface Area
High Flux Dialyzer is designed for hemodialysis treatments requiring increased convective clearance. High-flux membranes typically offer larger pore sizes and higher ultrafiltration coefficients to support enhanced middle-molecule removal. Procurement decisions focus on membrane material, surface area, and compatibility with existing machine transmembrane pressure ranges. Clinics select high-flux models to match prescribed treatment protocols and patient clearance targets.
Compatibility & Consumable Dependency
Dialyzers must be mechanically and hydraulically compatible with the clinic's dialysis machines and bloodline connectors. Selection includes checking priming volume, recommended blood flow ranges, and connector interface. Procurement should align dialyzer inventory with machine models and clinician preferences to avoid cross-compatibility issues.
Heparin Sodium Injection — 25000 IU
Strength, Dosage Form & Pack Configuration
Heparin Sodium Injection 25,000 IU is a high-strength anticoagulant formulation used in clinical settings, including dialysis and surgical procedures where institutional anticoagulation protocols require concentrated vials. Procurement teams typically request the exact vial size and presentation when sourcing to ensure compatibility with infusion and dosing workflows. Confirm the licensed commercial presentation when submitting an RFQ.
Dosage-Form-Specific Handling & Administration Context
As a parenteral anticoagulant, handling follows institutional clinical and pharmacy procedures. Procurement and clinical teams coordinate on storage, administration, and documentation aligned with local protocols.
On and Off Kit
Membrane, Flux Class & Surface Area
The On and Off Kit is a consumable accessory kit designed to support dialysis session setup and disconnection workflows. It typically contains connection fittings and single-use components to enable safe and efficient patient circuit management. Dialysis centres procure these kits to standardize session setup and minimize connection errors during routine hemodialysis operations.
Compatibility & Consumable Dependency
The kit is selected for compatibility with specific dialysis machine connectors and bloodlines. Procurement should confirm connector types and required component specifications when ordering.
Infusion Set / Saline Giving Set + Normal Saline
Material, Biocompatibility & Sterility
The Infusion Set supplied with Normal Saline is intended for IV administration and routine fluid therapy in clinical environments. The combined offering simplifies procurement by pairing a sterile IV set with a normal saline pack for immediate clinical use. Hospital and dialysis procurement teams commonly source such kits to streamline administration workflows and reduce preparation time at the point of care.
Design, Format & Packaging
The set includes standard connectors and is designed for single-use clinical administration. Packaging and configuration are selected to support sterile delivery and ease of use in inpatient and outpatient settings.
Cold Sterilant
Material, Biocompatibility & Sterility
Cold Sterilant is a chemical solution used for low-temperature sterilization and reprocessing of medical instruments and device components. It enables sterilization where heat-based methods are unsuitable. Clinical reprocessing and dialysis teams procure such sterilants to maintain device hygiene while protecting heat-sensitive equipment. Selection is guided by compatibility with device materials and institutional reprocessing protocols.
Design, Format & Packaging
Sterilant is supplied in defined concentrate or ready-to-use formats and packaged to meet handling and storage needs. Procurement should confirm preferred concentration and pack size when requesting quotes.
Disinfectant for Haemodialysis Machine
Membrane, Flux Class & Surface Area
The disinfectant for haemodialysis machines is formulated for effective cleaning and microbiological control of dialysis circuits and machine surfaces. It is selected for compatibility with dialysis components and for use within standard machine reprocessing cycles. Dialysis centres and hospital biomedical teams procure this product to maintain infection-control protocols and machine hygiene between sessions.
Compatibility & Consumable Dependency
Selection requires confirmation of material compatibility with internal machine components and membranes. Procurement should specify machine models and materials to confirm suitability.
Sodium Bicarbonate — Bag
Membrane, Flux Class & Surface Area
Sodium Bicarbonate Bag is the standard alkaline concentrate component used to prepare dialysate bicarbonate solutions at hemodialysis facilities. The bag format supports direct addition to mixing systems or automated bicarbonate mixers. Procurement teams value consistent assay and soluble profile to avoid precipitation during mixing. This bag form is sized for in-center mixing systems and aligns with institutional handling and dosing workflows, helping dialysis centers maintain predictable dialysate composition.
Compatibility & Consumable Dependency
The sodium bicarbonate bag integrates with standard bicarbonate mixers, pedestal mixers, and inline dosing systems. It is compatible with common dialysate concentrate Part I/Part II configurations when used per supplier instructions. Hospitals and dialysis centers typically pair these bags with RO-treated water and delivery manifolds. Bulk pack formats reduce handling frequency and streamline replenishment for high-volume clinics.
Sodium Bicarbonate — Cart
Membrane, Flux Class & Surface Area
Sodium Bicarbonate Cart is a transportable concentrate container intended for facilities using cart-fed bicarbonate delivery or point-of-use mixing. The cart format optimizes handling when frequent replacement or mobile mixing is required. Clinical procurement teams select cart systems for ease of movement and reduced manual transfer steps. The product supports standard bicarbonate dosing regimens and is compatible with commonly used dialysis mixing equipment.
Compatibility & Consumable Dependency
The cart integrates with pedestal mixers and inline dosing heads and is suitable where bag-to-cart transfer logistics are in use. It pairs with acid concentrates and RO-treated water; compatibility checks are recommended during procurement to ensure fittings and connectors match existing infrastructure. The cart option reduces labor associated with repeated bag changes in busy clinics.
Haemodialysis Concentrated Powder — Part I + II
Membrane, Flux Class & Surface Area
Haemodialysis Concentrated Powder Part I + Part II supplies the acid and bicarbonate components used to generate dialysate on-site. Powdered concentrates are measured and reconstituted to the facility's dialysate formulation. They are often chosen to reduce shipping weight and avoid liquid transport issues. Clinical teams must confirm mixing ratios and solubility parameters to ensure a consistent dialysate composition per session.
Compatibility & Consumable Dependency
Two-part powder concentrates are compatible with central mixing stations and automated powder dissolvers. They require precise dosing and RO water quality for complete dissolution and low particulate output. When selecting powdered options, procurement should verify that dissolution times and filtration steps align with existing mixing equipment and staff handling protocols.
Concentrated Haemodialysis Solution — Part I + Part II
Membrane, Flux Class & Surface Area
Concentrated Haemodialysis Solution Part I + Part II provide the acid and bicarbonate components needed for standard dialysate generation. These concentrates are formulated to dissolve cleanly with RO water and are intended for use with facility mixing systems and dosing heads. Facilities evaluating concentrates should review final dialysate conductivity and pH stability after mixing to ensure compatibility with membrane flux characteristics.
Compatibility & Consumable Dependency
The two-part concentrate pairs with common acid concentrate systems and bicarbonate delivery setups. It is used alongside RO-treated water and standard dosing pumps. Procurement should verify connector compatibility and dissolution performance for automated mixers to minimize manual adjustments during peak operation hours.
AV Fistula Needle
Membrane, Flux Class & Surface Area
AV Fistula Needle is a single-use cannulation needle used for establishing vascular access during hemodialysis. Needles are procured by dialysis centers for routine cannulation and replacement. Selection depends on gauge, length, and bevel design to match patient access and staff preference. Procurement teams should align gauge and length choices with clinical protocols to ensure consistent flow and reduced insertion trauma.
Compatibility & Consumable Dependency
These needles are compatible with standard tubing and bloodline connectors used in dialysis machines. They form part of the consumable kit that includes tubing, clamps, and antiseptic dressings. Hospitals often buy needles in sterile sealed packs and track batch information for infection control and inventory management.
Syringes
Material, Biocompatibility & Sterility
Disposable syringes offered here are intended for clinical and dialysis applications where single-use sterile devices are required. These syringes are designed for safe administration workflows and compatibility with standard needles and catheter connections used in hospital and dialysis environments. Procurement teams for hospitals and clinics typically select sterile single-use syringes to meet infection-control protocols and streamline disposal workflows.
Design, Format & Packaging
Syringes are supplied in sealed sterile packs and configured by volume and tip type. They are suitable for routine clinical administration and dialysis-related procedures where disposable components reduce cross-contamination risk.
Iron Sucrose Injection USP (Ferobest)
Strength, Dosage Form & Pack Configuration
Iron Sucrose Injection USP is a finished-dose intravenous formulation intended for clinical use in iron-replacement therapy. The product title indicates USP monograph compliance in its labeling; procurement teams in hospitals and dialysis centres typically source this formulation for intravenous infusion protocols addressing iron-deficiency anemia. Buyers should reference the exact commercially supplied strength and pack configuration when requesting quotes as those details govern dosing and packaging requirements.
Dosage-Form-Specific Handling & Administration Context
As an injectable formulation, handling follows institutional infusion protocols. Procurement and clinical teams coordinate on storage, administration, and documentation requirements tied to intravenous therapy workflows.
Dialysis Catheter
Membrane, Flux Class & Surface Area
The dialysis catheter is designed to provide reliable vascular access for hemodialysis procedures. It integrates with standard bloodlines and connectors used in dialysis centres. Procurement teams select catheters based on lumen configuration, connector compatibility, and sterility assurance to ensure safe access and efficient blood flow during sessions. The product suits hospital dialysis units and outpatient dialysis centres requiring dependable vascular access devices.
Compatibility & Consumable Dependency
The catheter design focuses on connector compatibility and ease of integration with existing dialysis circuit components. Selection typically considers lumen size, preferred tip configuration, and compatibility with institutional bloodlines and connectors.
