Smith+Nephew
Dispositifs médicaux, fournitures de soins de santé et produits cliniques.
Smith+Nephew fabrique des dispositifs médicaux, des fournitures de soins de santé et des produits cliniques à partir de ses opérations de Watford. 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
- Watford, United Kingdom
- Founded
- 1856
- Website
- smith-nephew.com
- Categories
- Fournitures médicales et de santé, Fournitures industrielles
- Markets
- Royaume-Uni, États-Unis, Allemagne, Japon
Verified facts
- 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)
- domain-registered (green), checked 2026-09-04 Domain registry record
- sanctions-clear (green), checked 2026-09-04 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-09-04 Mail server of the company domain
- fda-registered (green), checked 2026-09-04 FDA
- debarment-clear (green), checked 2026-09-04 OpenSanctions
- registry-activity (green), checked 1937-02-17 Companies House free company data product (UK)
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- registered-since (green), checked 1937-02-17 Companies House free company data product (UK)
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)