Renishaw
Dispositifs médicaux, fournitures de soins de santé et produits cliniques.
Renishaw fabrique des dispositifs médicaux, des fournitures de soins de santé et des produits cliniques à partir de ses opérations de Wotton-under-Edge. La société fournit des acheteurs d'hôpitaux, des distributeurs cliniques, des systèmes de santé ou des clients exportateurs sur ses principaux marchés cotés.
- Type
- brand seeking distribution
- Location
- Wotton-under-Edge, United Kingdom
- Founded
- 1973
- Website
- renishaw.com
- Categories
- Fournitures médicales et de santé, Fournitures industrielles
- Markets
- Royaume-Uni, États-Unis, Allemagne, Chine
Verified facts
- domain-registered (green), checked 2026-09-04 Domain registry record
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- licensed-sponsor (green), checked 2026-08-12 UK Home Office register of licensed sponsors (workers)
- corporate-mail-on-domain (green), checked 2026-09-04 Mail server of the company domain
- debarment-clear (green), checked 2026-09-04 OpenSanctions
- sanctions-clear (green), checked 2026-09-04 OpenSanctions
- fda-registered (green), checked 2026-09-04 FDA
- registry-active-global (green), checked 2026-08-31 Environment Agency public registers (England)
- operating-permit (green), checked 2026-08-31 Environment Agency public registers (England)
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- 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)