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Vacuum Splints
EUDAMEDClass I (EU MDR)
Ref Vacuum Splint Forearm Blue Line GE
by AB Germa
Identity
- Device Name
- Vacuum Splints EUDAMED
- Model / Reference
- Vacuum Splint Forearm Blue Line GE EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07350019591703 EUDAMED
- Basic UDI-DI
- 735001959P02VACSPLIGQ EUDAMED
- Direct Marketing DI
- 07350019591703 EUDAMED
- EMDN Code
- V0804 PATIENT IMMOBILISERS (in diagnostic or therapeutic procedures) EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Sweden 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
Vacuum Splints by AB Germa — 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 | 735001959P02VACSPLIGQ | Class I | Active |
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Manufacturer
- Manufacturer
- AB Germa
- EUDAMED SRN
- SE-MF-000003932
Sources (1)
- EUDAMED 37a94eb1-1211-43f5-81a5-fd2636e0bc2a 61 fields · synced Jul 10, 2026