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Lightvision

EUDAMED

Class IIa (EU MDR)

Ref 567-13800-17Ref 567-13800-13Ref 567-13800-11

by Shimadzu Corporation

Identity

Trade Name
LIGHTVISION EUDAMED
Device Name
LIGHTVISION EUDAMED
Model / Reference
567-13800-17 EUDAMED
567-13800-13 EUDAMED
567-13800-11 EUDAMED

Identifiers

Primary DI / UDI-DI
04540217059805 EUDAMED
04540217059768 EUDAMED
04540217059744 EUDAMED
Basic UDI-DI
B-04540217059805 EUDAMED
B-04540217059768 EUDAMED
B-04540217059744 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 (3)

  • EUDAMED 4b115dec-c5a2-40e2-a7b8-c2764447f767 61 fields · synced Jul 26, 2026
  • EUDAMED e8d0c355-2414-406b-8cbb-484902c6aacc 61 fields · synced May 18, 2026
  • EUDAMED 0f6ecdf8-72ce-4800-8b1a-0257a5961414 61 fields · synced May 19, 2026