Identity
- Trade Name
- Vidasis® EUDAMED
- Device Name
- Sterile Hernia Graft EUDAMED
- Model / Reference
- SIS-HRP-8L-13×22 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06970426865252 EUDAMED
- Basic UDI-DI
- B-06970426865252 EUDAMED
- EMDN Code
- P900299 SURGICAL MESHES - OTHER EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Vidasis® by Beijing Biosis Healing Biological Technology Co., Ltd. — Class III — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-06970426865252 | Class III | Active |
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Manufacturer
- EUDAMED SRN
- CN-MF-000040931
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED 04486f1f-b904-4237-a9ed-25c5b4a0d633 61 fields · synced Oct 6, 2026