Bio-Rad Laboratories, Inc.
Производитель инструментов для ПЦР, электрофореза и qPCR для исследовательских лабораторий.
Bio-Rad производит лабораторное оборудование, включая системы ПЦР, оборудование для электрофореза и термоциклеры для ПЦР, используемые в лабораториях биологических наук и клинических исследований. Компания экспортирует продукцию по всему миру через лабораторных дистрибьюторов и прямые продажи.
- Type
- brand seeking distribution
- Location
- Hercules, United States
- Website
- bio-rad.com
- Categories
- Медицинские товары и расходники
- Markets
- Соединенные Штаты, Германия, Китай, Япония
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)