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KT-10024830BeGR

EUDAMED

Class IIb (EU MDR)

Ref KT-10024830BeGRModel NA

by Lumenis (Germany) GmbH

Identity

Model / Reference
NA EUDAMED
KT-10024830BeGR EUDAMED

Identifiers

Primary DI / UDI-DI
04260539181212 EUDAMED
Basic UDI-DI
426053918QSWTPGX EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class IIb 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: Device sterilization/disinfection container, reusable

KT-10024830BeGR by Lumenis (Germany) GmbH — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000007655

Sources (1)

  • EUDAMED f641e449-eacb-4861-9b49-8baa2008c71c 61 fields · synced Jul 14, 2026