Centrifuges Suppliers & Bulk Manufacturers
Available Forms: Laboratory centrifuges, Clinical centrifuges, Refrigerated centrifuges
Available Strengths: Ranging from small-capacity mini-centifuges to high-capacity, refrigerated units; with speeds from 1,000 to 50,000 rpm for various laboratory applications
Reference Brands: Eppendorf, Thermo Fisher Scientific, Hitachi, BD, Beckman Coulter
Category: Medical Devices
Centrifuges is available in Laboratory centrifuges, Clinical centrifuges, Refrigerated centrifuges and strengths such as Ranging from small-capacity mini-centifuges to high-capacity, refrigerated units; with speeds from 1,000 to 50,000 rpm for various laboratory applications. 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, Centrifuges 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) |
Centrifuges 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:
Centrifuges sold in the EU and US are regulated to ensure safety, performance, and manufacturing quality. In the US, FDA approval requires validation, safety testing, and GMP compliance. In the EU, CE marking certifies conformity with in vitro diagnostic (IVD) and medical device regulations. Devices undergo validation, validation, stability testing, and audits, with detailed documentation including safety profiles, performance data, and manufacturing practices. For licensing procedures, approved dossiers, and latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to reliable, safe centrifuges vital for clinical, laboratory, and research applications worldwide, supporting precise sample separation and diagnostic accuracy.
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