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Ac-10202210

EUDAMED

Class IIb (EU MDR)

Ref AC-10202210Model NA

by Lumenis Be LTD

Identity

Trade Name
M22TM Q-Switched Head EUDAMED
Model / Reference
NA EUDAMED
AC-10202210 EUDAMED

Identifiers

Primary DI / UDI-DI
07290117772744 EUDAMED
Basic UDI-DI
729011777QSWHPKU EUDAMED
EMDN Code
Z12011019 MULTI–PLATFORM LASER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Netherlands 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-10202210 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 (2)

  • EUDAMED 58488a86-8d3e-42de-8861-596de5ddf5da 61 fields · synced Jun 19, 2026
  • EUDAMED 09ac25c7-1e66-43ba-8776-0997c8c814cf 61 fields · synced Jun 19, 2026