Renishaw
Dispositivos médicos, suministros sanitarios y productos clínicos.
Renishaw fabrica dispositivos médicos, suministros sanitarios y productos clínicos en sus operaciones de Wotton-under-Edge. La empresa abastece a compradores de hospitales, distribuidores clínicos, sistemas de salud o clientes de exportación en sus mercados primarios listados.
- Type
- brand seeking distribution
- Location
- Wotton-under-Edge, United Kingdom
- Founded
- 1973
- Website
- renishaw.com
- Categories
- Suministros médicos y sanitarios, Suministros industriales
- Markets
- Reino Unido, Estados Unidos, Alemania, China
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)