← Back to catalogue

Allux-Q Plus

EUDAMED

Class IIb (EU MDR)

Ref AMI-CL-0332Model ALLUX-Q PLUS

by Ami Inc.

Identity

Trade Name
ALLUX-Q PLUS EUDAMED
Device Name
Q-Switched Nd:YAG Laser EUDAMED
Model / Reference
ALLUX-Q PLUS EUDAMED
AMI-CL-0332 EUDAMED

Identifiers

Primary DI / UDI-DI
08800042100193 EUDAMED
Basic UDI-DI
B-08800042100193 EUDAMED
EMDN Code
Z12011017 NEODYMIUM SURGICAL LASER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Poland 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-Q Plus 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 1a947876-f1a1-448b-903b-4e909eb8a49a 61 fields · synced Jul 13, 2026