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Mg

EUDAMED

Class I (EU MDR)

Ref FTIMGModel MG

by Fiberoptics Technology Incorporated

Identity

Trade Name
MG EUDAMED
Device Name
Medical Light Guide EUDAMED
Model / Reference
MG EUDAMED
FTIMG EUDAMED

Identifiers

Primary DI / UDI-DI
D-00862658000319J4 EUDAMED
Basic UDI-DI
B-00862658000319J4 EUDAMED
EMDN Code
L0318 INSTRUMENTS FOR SUPPORT OF SURGICAL DEVICES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Mg by Fiberoptics Technology Incorporated — 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
US-MF-000018020
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED 74b7c0fd-ecfd-4d9a-a03a-d2737a377961 61 fields · synced Jul 19, 2026