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KT-00011111Be

EUDAMED

Class I (EU MDR)

Ref KT-00011111BeModel NA

by Lumenis Be LTD

Identity

Model / Reference
NA EUDAMED
KT-00011111Be EUDAMED

Identifiers

Primary DI / UDI-DI
17290117771935 EUDAMED
Basic UDI-DI
729011777FMXTPSLB EUDAMED
EMDN Code
Z12011080 LASER SURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I 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

KT-00011111Be by Lumenis Be 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

Manufacturer
Lumenis Be LTD
EUDAMED SRN
IL-MF-000022063
Authorised Representative
Lumenis (Germany) GmbH DE-AR-000007699

Sources (1)

  • EUDAMED 833e85c4-c008-4f8f-91b9-527f702f56d3 61 fields · synced Jun 18, 2026