Arjo AB
Arjo develops and manufactures patient handling equipment and medical devices for hospitals and c…
Arjo develops and manufactures patient handling equipment and medical devices for hospitals and care homes, ceiling hoists, mobile lifts, shower and bathing systems, pressure injury prevention mattresses, and medical beds. Headquartered in Malmö, Arjo markets its products directly to healthcare procurement bodies across Europe, North America, Australia, and Japan, supporting ageing-population care infrastructures.
- Type
- brand seeking distribution
- Location
- Malmö, Sweden
- Founded
- 1957
- Website
- arjo.com
- Categories
- Medical & Healthcare Supplies, Home Appliances
- Markets
- United States, United Kingdom, Germany, Sweden, Australia, Japan, France
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)