Iv Fluids And Blood Collection Sets Suppliers & Bulk Manufacturers
Available Forms: Lancets: Single-use, sterile, different gauges, Pen Needles: Disposable, sterile, various gauges and lengths for insulin pens
Available Strengths: Gauges range from 26G to 33G; needle lengths from 1/4 inch to 5/16 inch; sterile, single-use
Reference Brands: BD Microtainer, Medline, Sperian, SureGrip, BD Ultra-Fine, Novo Nordisk
Category: Medical Devices
IV fluids and blood collection sets is available in Lancets: Single-use, sterile, different gauges, Pen Needles: Disposable, sterile, various gauges and lengths for insulin pens and strengths such as Gauges range from 26G to 33G; needle lengths from 1/4 inch to 5/16 inch; sterile, single-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 fluids and blood collection 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 fluids and blood collection 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 fluids and blood collection sets in the EU and US are regulated to ensure safety, efficacy, and manufacturing quality. In the US, FDA approval requires validation, safety testing, and GMP compliance. In the EU, CE marking certifies conformity with the IVDR and medical device regulations. These devices undergo validation, stability testing, and audits, with comprehensive documentation including safety profiles, performance data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to reliable, safe IV fluids and blood collection sets, vital for effective patient care, diagnostics, and blood transfusion safety worldwide.
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