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Tray and lid KeriFuse

EUDAMED

Class I (EU MDR)

Ref 71/4-KERI

by Keri Medical SA

Identity

Trade Name
Tray and lid KeriFuse EUDAMED
Device Name
Tray/lid KeriFlex, rack+lid KeriFuse EUDAMED
Model / Reference
71/4-KERI EUDAMED

Identifiers

Primary DI / UDI-DI
07640181161829 EUDAMED
Basic UDI-DI
764018116007B8 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

Tray and lid KeriFuse 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 2d67c70c-57eb-47a9-9b11-cd19b2179de8 61 fields · synced Sep 17, 2026