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Lightvision

EUDAMED

Class IIa (EU MDR)

Ref 567-13800-12

by Shimadzu Corporation

Identity

Trade Name
LIGHTVISION EUDAMED
Device Name
LIGHTVISION EUDAMED
Model / Reference
567-13800-12 EUDAMED

Identifiers

Primary DI / UDI-DI
04540217059751 EUDAMED
Basic UDI-DI
B-04540217059751 EUDAMED
EMDN Code
Z12011101,Z12029007 EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Lightvision by Shimadzu Corporation — Class IIa — 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
JP-MF-000025145
Authorised Representative
Shimadzu Europa GmbH DE-AR-000013563

Sources (1)

  • EUDAMED 06b05f39-6d20-4a12-9a63-7c99c811e5a6 61 fields · synced Jun 19, 2026