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Rex-Q

EUDAMED

Class IIb (EU MDR)

Ref AMI-CL-0331AModel REX-Q

by Ami Inc.

Identity

Trade Name
REX-Q EUDAMED
Device Name
Q-Switched Nd:YAG Laser EUDAMED
Model / Reference
REX-Q EUDAMED
AMI-CL-0331A EUDAMED

Identifiers

Primary DI / UDI-DI
08800042100179 EUDAMED
Basic UDI-DI
B-08800042100179 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

Rex-Q 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 89125944-8866-41c4-910a-69f4269cbf6e 61 fields · synced Jun 20, 2026