Arjo AB
Arjo는 병원 및 의료기관용 환자 취급 장비와 의료 기기를 개발 및 제조합니다.
Arjo는 병원 및 요양원용 환자 취급 장비와 의료 기기, 천장 호이스트, 이동식 리프트, 샤워 및 목욕 시스템, 욕창 방지 매트리스, 의료용 침대를 개발 및 제조합니다. 말뫼에 본사를 둔 Arjo는 유럽, 북미, 호주, 일본 전역의 의료 조달 기관에 제품을 직접 판매하여 노인 인구 관리 인프라를 지원합니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Malmö, Sweden
- Founded
- 1957
- Website
- arjo.com
- Categories
- 의료 및 건강 관리 용품, 가전제품
- Markets
- 미국, 영국, 독일, 스웨덴, 오스트레일리아, 일본, 프랑스
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)