Medartis
骨科植入物、板、螺钉和手术系统。
Medartis 在巴塞尔工厂生产矫形植入物、钢板、螺钉和手术系统。该公司在其上市主要市场上为医疗保健系统、实验室、OEM 合作伙伴或受监管的出口客户提供服务。
- Type
- Manufacturer
- Location
- Basel, Switzerland
- Founded
- 1997
- Website
- medartis.com
- Categories
- 医疗保健用品
- Markets
- 瑞士, 美国, 德国, 日本
Verified facts
- lei-active (green), checked 2026-08-07 GLEIF global LEI register (golden copy)
- domain-registered (green), checked 2026-07-28 Domain registry record
- 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)
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)