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Modular Head Impactor - Body

EUDAMED

Class I (EU MDR)

Ref 4250-2031

by Enztec Limited

Identity

Trade Name
Modular Head Impactor - Body EUDAMED
Device Name
Impactors - General EUDAMED
Model / Reference
4250-2031 EUDAMED

Identifiers

Primary DI / UDI-DI
09421028113892 EUDAMED
Basic UDI-DI
942102811GMN001526 EUDAMED
Direct Marketing DI
09421028113892 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

Modular Head Impactor - Body 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 7415a087-081f-4cfd-bd08-91761ed72ddf 61 fields · synced Jul 8, 2026