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Gl6040

EUDAMED

Class I (EU MDR)

Ref 474-1810

by Zumax Medical CO., LTD.

Identity

Trade Name
GL6040 EUDAMED
Device Name
Illuminator EUDAMED
Model / Reference
474-1810 EUDAMED

Identifiers

Primary DI / UDI-DI
06945095544692 EUDAMED
Basic UDI-DI
69450955illuminatorXY EUDAMED
EMDN Code
Z12010702 MOBILE SCIALYTIC LAMPS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Gl6040 by Zumax Medical Co., LTD — 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

EUDAMED SRN
CN-MF-000011126
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 5e29dc3f-173d-44d5-94e4-22cd2d5f13e6 61 fields · synced Oct 6, 2026