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Sonorama

by Ids Ltd.

Ref IDS-UM-0831Model SONORAMA

Sonorama (IDS-UM-0831) is a medical device (EU MDD Class IIb; EMDN category ultrasound therapy equipment) made by Ids Ltd., registered in EUDAMED on 28 Apr 2026 (Basic UDI-DI B-08809578390276), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08809578390276 Basic UDI-DI 08809578390276UDI-DIDate28 Apr 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
High Intensity Focused Ultrasound
Model / reference
SONORAMA, IDS-UM-0831
Primary DI / UDI-DI
08809578390276
Basic UDI-DI
B-08809578390276
EMDN code
Z120610 Ultrasound therapy equipment
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
Spain

Manufacturer details

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

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Properties

Other properties (12, all answered No)