Bio-Rad Laboratories, Inc.
Fabricant d'instruments de PCR, d'électrophorèse et de qPCR pour les laboratoires de recherche.
Bio-Rad fabrique des instruments de laboratoire, notamment des systèmes PCR, des équipements d'électrophorèse et des thermocycleurs qPCR utilisés dans les laboratoires de sciences de la vie et de recherche clinique. L'entreprise exporte dans le monde entier via des distributeurs de laboratoire et des ventes directes.
- Type
- brand seeking distribution
- Location
- Hercules, United States
- Website
- bio-rad.com
- Categories
- Fournitures médicales et de santé
- Markets
- États-Unis, Allemagne, Chine, Japon
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-05 Mail server of the company domain
- domain-registered (green), checked 2026-08-05 Domain registry record
- market-access-eu (green), checked 2026-08-22 TRACES NT, European Commission register of approved establishments (DG SANTE)
- manufacturing-practice-certified (green), checked 2026-08-21 ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
- debarment-clear (green), checked 2026-08-05 OpenSanctions
- sanctions-clear (green), checked 2026-08-05 OpenSanctions
- fda-registered (green), checked 2026-08-05 FDA
- web-presence-since (green), checked 2026-08-05 Internet Archive (Wayback)
- facility-registered (green), checked 2026-08-07 US EPA Facility Registry Service (national combined file)
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- industrial-permit (green), checked 2026-08-23 ECHO, Enforcement and Compliance History Online (U.S. Environmental Protection Agency)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- FDA Registered FDA Establishment Registration
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)