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AutoSeal Hemostasis Valve Kit
EUDAMEDClass IIa (EU MDR)
Ref 20109500Ref 20109500-1
Identity
- Device Name
- AutoSeal Hemostasis Valve Kit EUDAMED
- Model / Reference
- 20109500 EUDAMED20109500-1 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06970226523505 EUDAMED06970226524229 EUDAMED
- Basic UDI-DI
- 697022652106FQ EUDAMED
- EMDN Code
- C900180 HAEMOSTASIS SYSTEMS - ACCESSORIES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Cyprus 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
AutoSeal Hemostasis Valve Kit by Curatia Medical Limited — 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 | 697022652106FQ | Class IIa | Active |
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Manufacturer
- Manufacturer
- Curatia Medical Limited
- EUDAMED SRN
- CN-MF-000015976
- Authorised Representative
- MedNet EC-REP III GmbH DE-AR-000011191
Sources (2)
- EUDAMED c8ec3478-a062-4722-b77b-3b979d0aba2b 61 fields · synced Oct 6, 2026
- EUDAMED a1e6e74c-d414-4904-8a07-9974638ffa71 61 fields · synced Jul 12, 2026