05059441401148
SARA FLEX
ArjoHuntleigh AB·Class I·EU EUDAMED·Trade name: Maxi Move 5Yes
Device classification
- Risk class
- Class I
- CND nomenclatures code
- V0805030102
- Trade name
- Maxi Move 5
- Implantable
- No
- Reusable
- No
- Measuring function
- No
Registration information
- Primary DI
- 05059441401148
- Basic UDI
- 5060693520112VK
- Version date
- March 07, 2025
- Manufacturer last update
- February 03, 2025
- Active status
- Yes
Manufacturer
- Manufacturer name
- ArjoHuntleigh AB
- Country
- Sweden
- Country type
- EU_MEMBER_STATE
- Address
- Hans Michelsensgatan 10 Malmö
- info@arjo.com
Regulatory information
- Competent authority
- Swedish Medical Products Agency
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Austria
- Market available
- Austria:None~None, Belgium:None~None, France:None~None, Germany:None~None, Italy:None~None, Netherlands:None~None
Device characteristics
- Human tissues
- No
- Animal tissues
- No
Device description (EMDN)
ELECTRIC MOBILE LIFTS
About this record
Access comprehensive regulatory information for SARA FLEX in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 05059441401148 and manufactured by ArjoHuntleigh AB in Sweden.
This page provides complete registration details including trade name (Maxi Move 5), manufacturer information, competent authority (Swedish Medical Products Agency), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.