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Aleste Combi

EUDAMED

Class IIb (EU MDR)

Ref IDS-UM-0651Model ALESTE COMBI

by Ids Ltd.

Identity

Trade Name
ALESTE COMBI EUDAMED
Device Name
Alexandrite&Long Pulsed Nd:YAG Laser EUDAMED
Model / Reference
ALESTE COMBI EUDAMED
IDS-UM-0651 EUDAMED

Identifiers

Primary DI / UDI-DI
08809578390368 EUDAMED
Basic UDI-DI
B-08809578390368 EUDAMED
EMDN Code
Z12011012 DYE/ALEXANDRITE 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

Aleste Combi 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 c23b7a7c-1f34-4741-a132-1dbf9c5a5304 61 fields · synced Jul 12, 2026