Identity
- Trade Name
- CITOTEST EUDAMED
- Device Name
- Tourniquet EUDAMED
- Model / Reference
- ABS EUDAMED5870-0004 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06975085645122 EUDAMED
- Basic UDI-DI
- 697079159TOU1001A00NUJ EUDAMED
- EMDN Code
- V9003 TOURNIQUETS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria 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
Citotest by Citotest Labware Manufacturing Co., Ltd — Class I — CE/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 | 697079159TOU1001A00NUJ | Class I | Active |
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Manufacturer
- Manufacturer
- Citotest Labware Manufacturing Co., Ltd
- EUDAMED SRN
- CN-MF-000017214
- Authorised Representative
- Wellkang Ltd XI-AR-000001836
Sources (1)
- EUDAMED a26237c1-d49b-4c85-b78c-f9798b62694c 61 fields · synced Oct 6, 2026