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ALLUX Nd:YAG

EUDAMED

Class IIb (EU MDR)

Ref AMI-CL-0613Model ALLUX Nd:YAG

by Ami Inc.

Identity

Trade Name
ALLUX Nd:YAG EUDAMED
Device Name
Long Pulsed Nd:YAG Laser EUDAMED
Model / Reference
ALLUX Nd:YAG EUDAMED
AMI-CL-0613 EUDAMED

Identifiers

Primary DI / UDI-DI
08800042100056 EUDAMED
Basic UDI-DI
B-08800042100056 EUDAMED
EMDN Code
Z12011012 DYE/ALEXANDRITE SURGICAL LASER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

ALLUX Nd:YAG by Ami Inc. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Ami Inc.
EUDAMED SRN
KR-MF-000017522
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED eae257f7-f56b-4c3e-a947-bec17fe5fa50 61 fields · synced Jul 9, 2026