Identity
- Trade Name
- Fotkudde EUDAMED
- Device Name
- Fotkudde EUDAMED
- Model / Reference
- 20000 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07350142990213 EUDAMED
- Basic UDI-DI
- 73501429920000MP EUDAMED
- Direct Marketing DI
- 07350142990213 EUDAMED
- EMDN Code
- V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER 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
Fotkudde by Adaptis Spektra AB — 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European Union No Longer Active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| EUDAMED | European Union | CE/MDR | 73501429920000MP | Class I | No Longer Active |
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Manufacturer
- Manufacturer
- Adaptis Spektra AB
- EUDAMED SRN
- SE-MF-000025764
Sources (1)
- EUDAMED bdd9bb45-3dcf-47cd-8955-1ba990346696 61 fields · synced Jul 19, 2026