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Modular Revision Trial

EUDAMED

Class I (EU MDR)

Ref MMP 07-2Model Metrimed Hip Instrument

by Metrimed Orvosi Műszergyártó Kft.

Identity

Device Name
Modular Revision Trial EUDAMED
Model / Reference
Metrimed Hip Instrument EUDAMED
MMP 07-2 EUDAMED

Identifiers

Primary DI / UDI-DI
05999154306937 EUDAMED
Basic UDI-DI
B-05999154306937 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Hungary 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

Modular Revision Trial by Metrimed Orvosi Műszergyártó Kft. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
HU-MF-000004640

Sources (1)

  • EUDAMED de4a42da-d90e-4bac-9c83-b4f8fa93fc50 61 fields · synced Sep 17, 2026