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Aesculap

EUDAMED

Class IIa (EU MDR)

Ref OP951

by Aesculap AG

Identity

Trade Name
Aesculap EUDAMED
Device Name
WL/FI light source EUDAMED
Model / Reference
OP951 EUDAMED

Identifiers

Primary DI / UDI-DI
04046955671748 EUDAMED
Basic UDI-DI
40392390000024272M EUDAMED
EMDN Code
Z12020402 LIGHT SOURCES FOR ENDOSCOPY AND MINIMALLY INVASIVE SURGERY 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

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

Category: Endoscopic light source unit, line-powered

Aesculap by Aesculap AG — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic light source unit, line-powered.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (1)

  • EUDAMED fcddbea7-d696-4d13-9a9f-606731e7a1da 61 fields · synced May 23, 2026