Identity
- Trade Name
- URGO K2 EUDAMED
- Device Name
- URGO K2 - URGO KTwo EUDAMED
- Model / Reference
- 600725 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03546890037544 EUDAMED
- Basic UDI-DI
- 354689UM00314T EUDAMED
- EMDN Code
- M03040199 ELASTIC COMPRESSION BANDAGES - 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
Yes
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
Urgo K2 by Laboratoires Urgo — 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 | 354689UM00314T | Class I | Active |
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Manufacturer
- Manufacturer
- Laboratoires Urgo
- EUDAMED SRN
- FR-MF-000002559
Sources (1)
- EUDAMED dd668bb4-e695-4331-8e36-f62fe2d707b9 61 fields · synced May 22, 2026