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Q-Las

EUDAMED

Class IIb (EU MDR)

Ref LS09002-LLZSModel LS09002

by A.R.C. Laser GmbH

Identity

Trade Name
Q-Las EUDAMED
Device Name
Q-Las EUDAMED
Model / Reference
LS09002 EUDAMED
LS09002-LLZS EUDAMED

Identifiers

Primary DI / UDI-DI
04260155593321 EUDAMED
Basic UDI-DI
426015559Q-LAS3H EUDAMED
Direct Marketing DI
04260155593321 EUDAMED
EMDN Code
Z12011017 NEODYMIUM 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

Q-Las by A.R.C. Laser GmbH — 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
A.R.C. Laser GmbH
EUDAMED SRN
DE-MF-000009383

Sources (1)

  • EUDAMED 60745055-a26b-47a5-83d0-65dc7f476821 61 fields · synced Jun 19, 2026