Arjo AB
Arjo sviluppa e produce apparecchiature per la movimentazione dei pazienti e dispositivi medici per ospedali e c...
Arjo sviluppa e produce attrezzature per la movimentazione dei pazienti e dispositivi medici per ospedali e case di cura, sollevatori a soffitto, sollevatori mobili, sistemi per docce e bagni, materassi per la prevenzione delle lesioni da pressione e letti medici. Con sede a Malmö, Arjo commercializza i suoi prodotti direttamente agli enti di approvvigionamento sanitario in Europa, Nord America, Australia e Giappone, supportando le infrastrutture di assistenza per la popolazione che invecchia.
- Type
- brand seeking distribution
- Location
- Malmö, Sweden
- Founded
- 1957
- Website
- arjo.com
- Categories
- Forniture medicali e sanitarie, Elettrodomestici
- Markets
- Stati Uniti, Regno Unito, Germania, Svezia, Australia, Giappone, Francia
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 2026-08-23 GLEIF global LEI register (golden copy)
Claimed certifications
- 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)