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Ikepgm

by Innovamedica S.p.A.

Ref IKEPGM

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805621668IKEPGMFM Basic UDI-DI 08056216680408UDI-DIDate6 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
IKEPGM
Primary DI / UDI-DI
08056216680408
Basic UDI-DI
805621668IKEPGMFM
EMDN Code
G020599, L1204
Device Class
Class I
Medical Purpose
KIT PER LA RIMOZIONE DEL PALLONCINO INTRAGASTRICO

Manufacturer details

EUDAMED SRN
IT-PR-000044913

Other devices from Innovamedica S.p.A.

See all devices from Innovamedica S.p.A. →

Properties

Other properties (1)

  • Sterile: No