Specimen Collection Containers Suppliers & Bulk Manufacturers
Available Forms: Vacutainer tubes, Sterile specimen jars, Swab containers, Transport media bottles
Available Strengths: Variety of sterile, leak-proof containers; tubes with different additives for blood, urine, or swab samples; sizes from 1 mL to 50 mL, CE and FDA approved
Reference Brands: BD, Greiner Bio-One, Fisher Scientific, Copan
Category: Medical Devices
Specimen collection containers is available in Vacutainer tubes, Sterile specimen jars, Swab containers, Transport media bottles and strengths such as Variety of sterile, leak-proof containers; tubes with different additives for blood, urine, or swab samples; sizes from 1 mL to 50 mL, CE and FDA approved. 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, Specimen collection containers 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) |
Specimen collection containers 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:
Specimen collection containers in the EU and US are regulated to ensure safety, sample integrity, and efficacy. In the US, FDA approval requires validation, safety testing, and GMP compliance, while in the EU, CE marking certifies conformity with in vitro diagnostic standards. 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 reliable, high-quality containers for accurate diagnostics, infection control, and disease monitoring in healthcare and veterinary applications worldwide, supporting efficient sample handling and diagnostic accuracy across regions.
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