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Ac-2009595gr

EUDAMED

Class I (EU MDR)

Ref AC-2009595GRModel NARef AC-2009599GR

by Lumenis (Germany) GmbH

Identity

Model / Reference
NA EUDAMED
AC-2009595GR EUDAMED
AC-2009599GR EUDAMED

Identifiers

Primary DI / UDI-DI
04260539180796 EUDAMED
04260539181762 EUDAMED
Basic UDI-DI
426053918FMADPT8P EUDAMED
426053918FMTPSB7 EUDAMED
EMDN Code
Z12011080 LASER SURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
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

Ac-2009595gr by Lumenis (Germany) GmbH — 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

EUDAMED SRN
DE-MF-000007655

Sources (2)

  • EUDAMED b07190ec-ba61-498e-929b-eca4d0061dc1 61 fields · synced Jul 17, 2026
  • EUDAMED 33bc17bc-a0e9-470a-b04c-3e2d77db1eb4 61 fields · synced Jul 17, 2026