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Q-Max Premium

EUDAMED

Class IIb (EU MDR)

Ref IDS-UM-0351AModel Q-MAX PREMIUM

by Ids Ltd.

Identity

Trade Name
Q-MAX PREMIUM EUDAMED
Device Name
Q-Switched Nd:YAG Laser EUDAMED
Model / Reference
Q-MAX PREMIUM EUDAMED
IDS-UM-0351A EUDAMED

Identifiers

Primary DI / UDI-DI
08809578390115 EUDAMED
Basic UDI-DI
B-08809578390115 EUDAMED
EMDN Code
Z12011017 NEODYMIUM SURGICAL LASER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain 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

Q-Max Premium by Ids Ltd. — 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
Ids Ltd.
EUDAMED SRN
KR-MF-000018259
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED f72e1fa9-6eca-4b18-8620-cfe4630f0c3b 61 fields · synced Jun 18, 2026