Arjo AB
Arjo, hastaneler ve klinikler için hasta taşıma ekipmanları ve tıbbi cihazlar geliştirmekte ve üretmektedir.
Arjo, hastaneler ve bakım evleri için hasta taşıma ekipmanları ve tıbbi cihazlar, tavan vinçleri, mobil asansörler, duş ve banyo sistemleri, basınç yaralanmalarını önleyici yataklar ve tıbbi yataklar geliştirmekte ve üretmektedir. Merkezi Malmö'de bulunan Arjo, ürünlerini doğrudan Avrupa, Kuzey Amerika, Avustralya ve Japonya'daki sağlık hizmeti satın alma kurumlarına pazarlayarak yaşlanan nüfusa yönelik bakım altyapılarını destekliyor.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Malmö, Sweden
- Founded
- 1957
- Website
- arjo.com
- Categories
- Tıbbi ve Sağlık Malzemeleri, Ev Aletleri
- Markets
- Amerika Birleşik Devletleri, Birleşik Krallık, Almanya, İsveç, Avustralya, Japonya, Fransa
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
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
- domain-registered (green), checked 2026-08-04 Domain registry record
- debarment-clear (green), checked 2026-08-04 OpenSanctions
- lei-lapsed (amber), checked 2026-08-04 GLEIF
- sanctions-clear (green), checked 2026-08-04 OpenSanctions
- 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 9001, Quality Management IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- ISO 45001, Occupational Safety IAF CertSearch
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)
- Consumer goods sold in the EU fall under the General Product Safety Regulation (GPSR, applies since 13 Dec 2024): a responsible person in the EU is mandatory. EUR-Lex: Regulation (EU) 2023/988 (GPSR)