Arjo AB
Arjo 为医院和社区开发和制造患者处理设备和医疗设备……
Arjo 为医院和疗养院开发和制造患者处理设备和医疗设备、天花板吊机、移动升降机、淋浴和沐浴系统、预防压力损伤床垫和医疗床。 Arjo 总部位于马尔默，直接向欧洲、北美、澳大利亚和日本的医疗保健采购机构销售其产品，支持老龄化人口护理基础设施。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Malmö, Sweden
- Founded
- 1957
- Website
- arjo.com
- Categories
- 医疗保健用品, 家电
- Markets
- 美国, 英国, 德国, 瑞典, 澳大利亚, 日本, 法国
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)