Identity
- Trade Name
- Vacuum Splint Forearm FW EUDAMED
- Device Name
- Vacuum Splints EUDAMED
- Model / Reference
- 23272007000 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07350019592090 EUDAMED
- Basic UDI-DI
- 735001959P02VACSPLIGQ EUDAMED
- Direct Marketing DI
- 07350019592090 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 Splint Forearm FW 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 9b7a7796-d412-4b6d-abe7-5c5d3c7c6880 61 fields · synced Jul 23, 2026