Identity
- Trade Name
- KREWI-Crepp EUDAMED
- Device Name
- 230 EUDAMED
- Model / Reference
- 501060 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04004221064298 EUDAMED
- Basic UDI-DI
- 4004221230WL EUDAMED
- Unit of Use DI
- 04004221020089 EUDAMED
- EMDN Code
- M030402010101 ELASTIC SUPPORT BANDAGES, NON-ADHESIVE, EXTENSIBLE IN ONE DIRECTION, HIGH EXTENSIBILITY 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
KREWI-Crepp by KOB 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 | 4004221230WL | Class I | Active |
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Manufacturer
- Manufacturer
- KOB GmbH
- EUDAMED SRN
- DE-MF-000005043
Sources (1)
- EUDAMED 9357f547-8c69-4024-8939-7da0b62fbdc0 61 fields · synced Sep 18, 2026