Identity
- Trade Name
- Ureterocutaneostomy catheter EUDAMED
- Device Name
- RÜSCH Ureterocutaneostomy Catheter EUDAMED
- Model / Reference
- 850281-000080 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 14026704737564 EUDAMED
- Basic UDI-DI
- 08019020000000000000187L3 EUDAMED
- EMDN Code
- U040302 URETEROCUTANEOSTOMY PROBES EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- Ireland 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
Ureterocutaneostomy catheter by Teleflex Medical — Class IIb — 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 | 08019020000000000000187L3 | Class IIb | Active |
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Manufacturer
- Manufacturer
- Teleflex Medical
- EUDAMED SRN
- IE-MF-000015868
Sources (1)
- EUDAMED a0b2d93a-7387-46d9-98f6-8e5fdf3cc6a4 61 fields · synced Jul 21, 2026