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AC-2005210Be

EUDAMED

Class IIa (EU MDR)

Ref AC-2005210BeModel NA

by Lumenis Be LTD

Identity

Model / Reference
NA EUDAMED
AC-2005210Be EUDAMED

Identifiers

Primary DI / UDI-DI
07290117770788 EUDAMED
Basic UDI-DI
729011777STRP4 EUDAMED
EMDN Code
Z12011080 LASER SURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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-2005210Be by Lumenis Be Ltd — Class IIa — 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 3eff353e-2766-448a-a52c-30459b7d4209 61 fields · synced Jul 20, 2026