Getinge
Systèmes de stérilisation, ventilateurs, équipements de salle d’opération et dispositifs de survie.
Getinge fabrique des systèmes de stérilisation, des ventilateurs, des équipements de salle d'opération et des dispositifs de survie à partir de ses opérations de Göteborg. 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
- Gothenburg, Sweden
- Founded
- 1904
- Website
- getinge.com
- Categories
- Fournitures médicales et de santé, Fournitures industrielles
- Markets
- Suède, Allemagne, États-Unis, Chine
Verified facts
- domain-registered (green), checked 2026-08-08 Domain registry record
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- lei-lapsed (amber), checked 2026-08-08 GLEIF
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- fda-registered (green), checked 2026-08-08 FDA
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
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)