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KeriFlex® - PIP Finger Joint Implant - PIP 0
EUDAMEDClass III (EU MDR)
Ref 210-P20000
Identity
- Trade Name
- KeriFlex® - PIP Finger Joint Implant - PIP 0 EUDAMED
- Device Name
- KeriFlex - MCP and PIP Finger Joint Implants EUDAMED
- Model / Reference
- 210-P20000 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07640181162017 EUDAMED
- Basic UDI-DI
- 764018116011AX EUDAMED
- EMDN Code
- P090403 HAND PROSTHESES INTERPHALANGE COMPONENTS EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
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
KeriFlex® - PIP Finger Joint Implant - PIP 0 by Keri Medical SA — Class III — 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 | 764018116011AX | Class III | 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 51f40358-b76e-47dd-8a0d-98ce3e2d412b 61 fields · synced Jun 17, 2026