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KITPOSE3ASTD

by Innovamedica S.p.A.

Ref KITPOSE3ASTD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805621668KITPOSE3ASTDK2 Basic UDI-DI 08056216680057UDI-DIDate6 Oct 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  • Withdrawn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
KITPOSE3ASTD
Primary DI / UDI-DI
08056216680057
Basic UDI-DI
805621668KITPOSE3ASTDK2
EMDN Code
G0280, G03080199, H020303
Device Class
Class IIb
Medical Purpose
KIT PLICATURA GASTRICA ENDOSCOPICA

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