Smith+Nephew
Медицинское оборудование, товары медицинского назначения и клиническая продукция.
Smith+Nephew производит медицинское оборудование, товары медицинского назначения и клиническую продукцию на своих предприятиях в Уотфорде. Компания снабжает покупателей больниц, клинических дистрибьюторов, системы здравоохранения или экспортных клиентов на своих перечисленных основных рынках.
- Type
- brand seeking distribution
- Location
- Watford, United Kingdom
- Founded
- 1856
- Website
- smith-nephew.com
- Categories
- Медицинские товары и расходники, Промышленные расходники
- Markets
- Великобритания, Соединенные Штаты, Германия, Япония
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)