Identity
- Trade Name
- PODOSCOPIO EUDAMED
- Device Name
- 6100 PODOSCOPIO EUDAMED
- Model / Reference
- PODOSCOPIO EUDAMED6100 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 8424591610004 EUDAMED
- Basic UDI-DI
- 8424591PDVH EUDAMED
- Direct Marketing DI
- 8424591610004 EUDAMED
- EMDN Code
- V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Spain 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
Podoscopio by Fabricados Triton, S.L. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union No Longer Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 8424591PDVH | Class I | No Longer Active |
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Manufacturer
- Manufacturer
- Fabricados Triton, S.L.
- EUDAMED SRN
- ES-MF-000018967
Sources (1)
- EUDAMED b2aa9149-00dd-40c5-bd25-d66585acf390 61 fields · synced Jun 17, 2026