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UDI Compass
Certificate valid

Snapshot 2026-10-11 · Link to EUDAMED

KeriFlex® - PIP Finger Joint Implant - PIP 0

UDI-DI 07640181162017Basic UDI-DI 764018116011AX

Class III · MDR · Keri Medical SA

Identification
Model
—
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
Yes
Measuring function
No
Reusable surgical
No
Certificates

286202031898

EU technical documentation assessment · valid

Notified body: Intertek Medical Notified Body AB (2862)

Valid from 2025-12-05 · Expiry 2028-02-15

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

Keri Medical SA

SRN CH-MF-000021960

CH · Plan-les-Ouates

manufacturer

Authorised representative: Keri Medical France (FR-AR-000009590)

Related UDI-DIs

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/keriflex-pip-finger-joint-implant-pip-0-2017 · UDI page: /udi/07640181162017

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