Iv Cannulas & Infusion Sets Suppliers & Bulk Manufacturers
Available Forms: IV cannulas: Plastic, sterile, straight; Infusion sets: Tubing, connectors, drip chambers
Available Strengths: Cannula sizes from 14G to 24G; infusion set drip chambers and tubing options for pediatric and adult use
Reference Brands: BD (Becton Dickinson), Bard (BD), Teleflex, Hospira
Category: Medical Devices
IV Cannulas & Infusion Sets is available in IV cannulas: Plastic, sterile, straight; Infusion sets: Tubing, connectors, drip chambers and strengths such as Cannula sizes from 14G to 24G; infusion set drip chambers and tubing options for pediatric and adult use. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, IV Cannulas & Infusion Sets is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.
| Technical Specifications & Supply Details | |
|---|---|
| Lead Time | 7 to 60 days (depending on batch size & schedule) |
| MOQ | As per manufacturer’s batch size |
| COA | Available with every batch |
| Regulatory Dossier / DMF | Available upon request |
| Export Documentation | FSC, COA, Manufacturing License, Product Permission |
| Standards | IP, BP, USP |
| Certifications | WHO-GMP, EU-GMP, USFDA (as applicable) |
IV Cannulas & Infusion Sets can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
Product Description:
IV cannulas and infusion sets are regulated in both the US and EU, supported by dossiers demonstrating safety, efficacy, and manufacturing quality in compliance with GMP standards. In the US, FDA approval involves clinical validation and safety assessments, while in the EU, CE marking certifies conformity with in vitro diagnostic and medical device regulations. These devices undergo validation, stability testing, and audits, with comprehensive documentation including safety profiles, clinical data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to safe, reliable infusion products for healthcare and veterinary use worldwide, supporting effective patient care.
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