Medartis
Implants orthopédiques, plaques, vis et systèmes chirurgicaux.
Medartis fabrique des implants orthopédiques, des plaques, des vis et des systèmes chirurgicaux depuis ses opérations de Bâle. La société fournit des systèmes de santé, des laboratoires, des partenaires OEM ou des clients exportateurs réglementés sur ses principaux marchés cotés.
- Type
- brand seeking distribution
- Location
- Basel, Switzerland
- Founded
- 1997
- Website
- medartis.com
- Categories
- Fournitures médicales et de santé
- Markets
- Suisse, États-Unis, Allemagne, Japon
Verified facts
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- places-goods-on-market (green), checked 2026-08-21 Swissmedic, swissdamed register of Swiss and Liechtenstein economic operators for medical devices
- registered-manufacturer (green), checked 2026-08-21 Swissmedic, swissdamed register of Swiss and Liechtenstein economic operators for medical devices
- domain-registered (green), checked 2026-07-28 Domain registry record
- operating-permit (green), checked 2026-07-24 SHAB, Swiss Official Gazette of Commerce
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- fda-registered (green), checked 2026-07-21 FDA
- registry-active-global (green), checked 2026-07-21 Zefix (Swiss commercial registry)
- sanctions-clear (green), checked 2026-07-21 OpenSanctions
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- FDA Registered FDA Establishment Registration
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)