SARA FLEX - EUDAMED Registration 05059441401179
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 05059441401179 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.
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EUDAMED Official Data
Class I
05059441401179
Yes
SARA FLEX
Trade Name: Maxi Move 5
Device Description (EMDN)
ELECTRIC MOBILE LIFTS
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
05059441401179
Basic UDI
5060693520112VK
Version Date
March 07, 2025
Manufacturer Last Update
February 03, 2025
Active Status
Yes
Manufacturer
Manufacturer Name
ArjoHuntleigh ABCountry
Sweden
Country Type
EU_MEMBER_STATE
Address
Hans Michelsensgatan 10 Malmö
Email
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