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Retractor Impactor

EUDAMED

Class I (EU MDR)

Ref MIH-026-00

by Enztec Limited

Identity

Trade Name
Retractor Impactor EUDAMED
Device Name
Minimally Invasive Hip (MIH) - Non-powered EUDAMED
Model / Reference
MIH-026-00 EUDAMED

Identifiers

Primary DI / UDI-DI
09421028114431 EUDAMED
Basic UDI-DI
942102811GMN002223 EUDAMED
Direct Marketing DI
09421028114431 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

Retractor Impactor 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 3676fcf7-8eb9-4a02-89f3-fbf6bf58e28e 61 fields · synced Jul 21, 2026