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Odyssey

by Ids Ltd.

Ref IDS-UM-0422Model ODYSSEY

Odyssey (IDS-UM-0422) is a medical device (EU MDD Class IIb; EMDN category carbon dioxide surgical laser) made by Ids Ltd., registered in EUDAMED on 3 Jul 2025 (Basic UDI-DI B-08809578390221), active as of 24 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08809578390221 Basic UDI-DI 08809578390221UDI-DIDate3 Jul 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Fractional CO2 Laser
Model / reference
ODYSSEY, IDS-UM-0422
Primary DI / UDI-DI
08809578390221
Basic UDI-DI
B-08809578390221
EMDN code
Z12011005 Carbon dioxide surgical laser
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
KR-MF-000018259
Authorised representative
Obelis s.a. BE-AR-000000106

Similar devices in this category

Other devices filed under CARBON DIOXIDE SURGICAL LASER.

Other devices from Ids Ltd.

See all devices from Ids Ltd. →

Properties

Other properties (12, all answered No)