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Kitfoagb

by Innovamedica S.p.A.

Ref KITFOAGB

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805621668KITFOAGB6B Basic UDI-DI 08056216680224UDI-DIDate1 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
KITFOAGB
Primary DI / UDI-DI
08056216680224
Basic UDI-DI
805621668KITFOAGB6B
EMDN Code
G020501, G020502, H02030106
Device Class
Class IIb
Medical Purpose
Bypass gastrico funzionale a singola anastomosi (FOAGB)

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