Ottobock
Протезирование, ортопедические изделия, инвалидные коляски и средства передвижения.
Ottobock производит протезы, ортопедические изделия, инвалидные коляски и товары для передвижения на своих предприятиях в Дудерштадте. Компания поставляет системы здравоохранения, лаборатории, OEM-партнерам или регулируемым экспортным клиентам на перечисленных основных рынках.
- Type
- brand seeking distribution
- Location
- Duderstadt, Germany
- Founded
- 1919
- Website
- ottobock.com
- Categories
- Медицинские товары и расходники
- Markets
- Германия, Соединенные Штаты, Япония, Австралия
Verified facts
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- vat-valid (green), checked 2026-08-03 VIES
- domain-registered (green), checked 2026-08-03 Domain registry record
- fda-registered (green), checked 2026-08-03 FDA
- media-mention (green), checked 2026-08-02 boerse-global.de
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
Profiles
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- FDA Registered FDA Establishment Registration
- AEO, Authorised Economic Operator EU AEO database
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)