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Ac-0013552

EUDAMED

Class IIb (EU MDR)

Ref AC-0013552Model NA

by Lumenis Be LTD

Identity

Model / Reference
NA EUDAMED
AC-0013552 EUDAMED

Identifiers

Primary DI / UDI-DI
07290117770962 EUDAMED
Basic UDI-DI
729011777UPASCNLQ EUDAMED
EMDN Code
Z12011005 CARBON DIOXIDE SURGICAL LASER 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

Ac-0013552 by Lumenis Be Ltd — Class IIb — 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 b32de0f5-36fc-4812-ab63-5e06ac73e907 61 fields · synced Jul 21, 2026