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CliniFix® Universal Hydrocolloid Securement Device
EUDAMEDClass I (EU MDR)
Ref 40-310
Identity
- Trade Name
- CliniFix® Universal Hydrocolloid Securement Device EUDAMED
- Device Name
- CliniFix® Universal Hydrocolloid Securement Device EUDAMED
- Model / Reference
- 40-310 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05017950000009 EUDAMED
- Basic UDI-DI
- 5017950CliniFixCP EUDAMED
- Direct Marketing DI
- 05017950000009 EUDAMED
- EMDN Code
- U0180 URETHRAL PROSTATIC AND BLADDER CATHETERS - ACCESSORIES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Ireland 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
CliniFix® Universal Hydrocolloid Securement Device by CliniMed Limited — 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 | 5017950CliniFixCP | Class I | Active |
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Manufacturer
- Manufacturer
- CliniMed Limited
- EUDAMED SRN
- GB-MF-000023784
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (1)
- EUDAMED f1729c42-3c26-4796-84ab-31a60d403197 61 fields · synced Jun 19, 2026