Getinge
Системы стерилизации, аппараты искусственной вентиляции легких, операционное оборудование и устройства жизнеобеспечения.
Компания Getinge производит системы стерилизации, аппараты искусственной вентиляции легких, оборудование для операционных и устройства жизнеобеспечения на своих предприятиях в Гетеборге. Компания снабжает покупателей больниц, клинических дистрибьюторов, системы здравоохранения или экспортных клиентов на своих перечисленных основных рынках.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Gothenburg, Sweden
- Founded
- 1904
- Website
- getinge.com
- Categories
- Медицинские товары и расходники, Промышленные расходники
- Markets
- Швеция, Германия, Соединенные Штаты, Китай
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
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 2026-09-07 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- 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)