Identity
- Trade Name
- KeriFix EUDAMED
- Device Name
- Suture anchor kit: Impacted anchor + Suture UHMWPE, USP 4.0 EUDAMED
- Model / Reference
- KeriFix EUDAMED500-B10002 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07640181160464 EUDAMED
- Basic UDI-DI
- B-07640181160464 EUDAMED
- EMDN Code
- H9099 SUTURE DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- France 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
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
KeriFix by Keri Medical SA — Class IIb — MDD — 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-07640181160464 | Class IIb | Active |
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Manufacturer
- Manufacturer
- Keri Medical SA
- EUDAMED SRN
- CH-MF-000021960
- Authorised Representative
- Keri Medical France FR-AR-000009590
Sources (1)
- EUDAMED 62bb1683-9fa5-45a6-b2de-d3cd2e033813 61 fields · synced Jun 18, 2026