Identity
- Trade Name
- UROMED Guide Wire »standard« EUDAMED
- Device Name
- GI01 EUDAMED
- Model / Reference
- 2732 EUDAMED2722 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250098805957 EUDAMED04250098805773 EUDAMED
- Basic UDI-DI
- 04250098810050EH EUDAMED
- EMDN Code
- U0602 UROLOGICAL GUIDEWIRES, NOT HYDROPHILIC EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
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
UROMED Guide Wire »standard« by UROMED Kurt Drews KG — Class IIa — 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 | 04250098810050EH | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- UROMED Kurt Drews KG
- EUDAMED SRN
- DE-MF-000006084
Sources (2)
- EUDAMED 72380289-09c4-43e3-8fb6-ef96bfe0217b 61 fields · synced Oct 6, 2026
- EUDAMED becfe228-6134-4618-881a-02863e386ae3 61 fields · synced May 17, 2026