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OCI Anvil+

EUDAMED

Class I (EU MDR)

Ref 4252-2303

by Enztec Limited

Identity

Trade Name
OCI Anvil+ EUDAMED
Device Name
Enztec Cup Impactors EUDAMED
Model / Reference
4252-2303 EUDAMED

Identifiers

Primary DI / UDI-DI
09421028116657 EUDAMED
Basic UDI-DI
942102811GMN00092B EUDAMED
Direct Marketing DI
09421028116657 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

OCI Anvil+ by Enztec Limited — 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
Enztec Limited
EUDAMED SRN
NZ-MF-000002264
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED c3d01db4-84e4-4649-8b8c-74600188a36c 61 fields · synced Jul 24, 2026