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Lid PIP

EUDAMED

Class I (EU MDR)

Ref ALX-KERI-5-002

by Keri Medical SA

Identity

Trade Name
Lid PIP EUDAMED
Device Name
Rack/lid KeriFlex EUDAMED
Model / Reference
ALX-KERI-5-002 EUDAMED

Identifiers

Primary DI / UDI-DI
07640181161836 EUDAMED
Basic UDI-DI
764018116008BA EUDAMED
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

Lid PIP by Keri Medical SA — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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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 ceb85bee-c633-4d14-ad59-cdca599880d1 61 fields · synced Jul 23, 2026