Identity
- Trade Name
- Maxi 500 EUDAMED
- Device Name
- SARA FLEX EUDAMED
- Model / Reference
- HEB0000 EUDAMEDKM560080-09 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05056097323534 EUDAMED
- Basic UDI-DI
- 5060693520112VK EUDAMED
- EMDN Code
- V0805030102 ELECTRIC MOBILE LIFTS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Maxi 500 by Arjohuntleigh AB — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 5060693520112VK | Class I | Active |
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Manufacturer
- Manufacturer
- ArjoHuntleigh AB
- EUDAMED SRN
- SE-MF-000000696
Sources (1)
- EUDAMED 19ec49fe-e538-4af2-9678-358129b44551 61 fields · synced Jun 18, 2026