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Liquick X-treme, Intermittent catheter, Ergothan tip, CH10, Female size
EUDAMEDClass I (EU MDR)
Ref 851822-000100
Identity
- Trade Name
- Liquick X-treme, Intermittent catheter, Ergothan tip, CH10, Female size EUDAMED
- Device Name
- Liquick X-Treme, Liquick X-Treme Plus EUDAMED
- Model / Reference
- 851822-000100 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 14026704743077 EUDAMED
- Basic UDI-DI
- 08019020000000000000175KU EUDAMED
- EMDN Code
- U010199 URETHRAL PROSTATIC AND BLADDER CATHETERS, NOT SELF-RETAINED - OTHER EUDAMED
Classification
- Device Class
- Class I 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
Liquick X-treme, Intermittent catheter, Ergothan tip, CH10, Female size by Teleflex Medical — 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 | 08019020000000000000175KU | Class I | Active |
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Manufacturer
- Manufacturer
- Teleflex Medical
- EUDAMED SRN
- IE-MF-000015868
Sources (1)
- EUDAMED 5d5b1ae1-ce4d-4399-a213-24a7c1c3db68 61 fields · synced Oct 6, 2026