Identity
- Trade Name
- KeriLock EUDAMED
- Device Name
- Suture anchor kit: Screwed anchor + Suture UHMWPE, USP 4.0 EUDAMEDSuture anchor kit: Screwed anchor + Suture UHMWPE, USP 2.0 EUDAMED
- Model / Reference
- KeriLock EUDAMED500-B20002 EUDAMED500-B20001 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07640181160495 EUDAMED07640181160488 EUDAMED
- Basic UDI-DI
- B-07640181160495 EUDAMEDB-07640181160488 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
KeriLock 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-07640181160495 | 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 (2)
- EUDAMED 143e13d0-f598-4a13-8846-72ba42ec84c0 61 fields · synced Oct 6, 2026
- EUDAMED 4501e84f-d450-4092-a558-da084db9a7cb 61 fields · synced May 18, 2026