Identity
- Trade Name
- KDM BioKlair Semana EUDAMED
- Device Name
- KDM BioKlair Semana EUDAMED
- Model / Reference
- 031101 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +E2510311011 EUDAMED
- Basic UDI-DI
- ++E251000605018N EUDAMED
- Direct Marketing DI
- +E2510311011 EUDAMED
- EMDN Code
- V0799 PRODUCTS FOR CLEANING MEDICAL DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
KDM BioKlair Semana by Alpro Medical Gmbh — 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 | ++E251000605018N | Class I | Active |
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Manufacturer
- Manufacturer
- Alpro Medical Gmbh
- EUDAMED SRN
- DE-MF-000010603
Sources (1)
- EUDAMED 1e8ef5e4-5a6a-4e0d-848d-35a7d726745d 61 fields · synced Oct 9, 2026