Identity
- Trade Name
- URGO K2 Lite Latex Free EUDAMED
- Device Name
- URGO K2 Lite Latex Free - URGO KTwo Reduced Latex Free EUDAMED
- Model / Reference
- 552937 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03546890029365 EUDAMED
- Basic UDI-DI
- 354689UM00785M 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
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
URGO K2 Lite Latex Free 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 | 354689UM00785M | Class I | Active |
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Manufacturer
- Manufacturer
- Laboratoires Urgo
- EUDAMED SRN
- FR-MF-000002559
Sources (1)
- EUDAMED 046a5789-218c-424a-9a32-980992198fe8 61 fields · synced Jun 19, 2026