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Pinacle

by Ids Ltd.

Ref IDS-UM-0961Model PINACLE

Pinacle (IDS-UM-0961) is a medical device (EU MDD Class IIb; EMDN category electrosurgical units (esu) for general use) made by Ids Ltd., registered in EUDAMED on 2 Jul 2025 (Basic UDI-DI B-08809578390252), 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-08809578390252 Basic UDI-DI 08809578390252UDI-DIDate2 Jul 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Electrosurgical Unit
Model / reference
PINACLE, IDS-UM-0961
Primary DI / UDI-DI
08809578390252
Basic UDI-DI
B-08809578390252
EMDN code
Z12010902 Electrosurgical units (esu) for general use
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
Greece

Manufacturer details

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

Related devices

Category: Foot-switch, electrical

Similar devices in this category

Other devices filed under ELECTROSURGICAL UNITS (ESU) FOR GENERAL USE.

Other devices from Ids Ltd.

See all devices from Ids Ltd. →

Properties

  • Supplied sterile
  • Sterilise before use
Other properties (10, all answered No)