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Hl8200

EUDAMED

Class I (EU MDR)

Ref 572-0040

by Zumax Medical CO., LTD.

Identity

Trade Name
HL8200 EUDAMED
Device Name
Headlight EUDAMED
Model / Reference
572-0040 EUDAMED

Identifiers

Primary DI / UDI-DI
06945095546535 EUDAMED
Basic UDI-DI
69450955headlight7K 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

Hl8200 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 3e16ece4-829e-4cdc-b2cb-1dc323a2d24f 61 fields · synced Aug 3, 2026