Getinge
Sistem sterilisasi, ventilator, peralatan ruang operasi dan perangkat pendukung kehidupan.
Getinge memproduksi sistem sterilisasi, ventilator, peralatan ruang operasi, dan perangkat pendukung kehidupan dari operasinya di Gothenburg. Perusahaan ini memasok pembeli rumah sakit, distributor klinis, sistem layanan kesehatan, atau pelanggan ekspor di seluruh pasar utama yang terdaftar.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Gothenburg, Sweden
- Founded
- 1904
- Website
- getinge.com
- Categories
- Perlengkapan Medis & Kesehatan, Perlengkapan Industri
- Markets
- Swedia, Jerman, Amerika Serikat, Tiongkok
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)