Identity
- Trade Name
- Footrise XS EUDAMED
- Device Name
- Pro Orthic Footrise EUDAMED
- Model / Reference
- PO 31802 EUDAMEDPO 31802 XS EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08718873005696 EUDAMED
- Basic UDI-DI
- 871887300573LC EUDAMED
- EMDN Code
- Y060406,Y06120601 EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Netherlands 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
Footrise XS by Lomed Nederland — 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 | 871887300573LC | Class I | Active |
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Manufacturer
- Manufacturer
- Lomed Nederland
- EUDAMED SRN
- NL-MF-000032807
Sources (1)
- EUDAMED 8e37fb05-ae08-4618-a479-827f780453dd 61 fields · synced Jul 29, 2026