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Kit Mano/Piede -K95

by So.Ge.Si. S.p.A.

Ref K95Model KIT PROCEDURALE DI TELERIA STERILIZZATO A VAPORE

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805567230KITTTRLF Basic UDI-DIDate17 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  • Withdrawn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
KIT PROCEDURALE DI TELERIA STERILIZZATO A VAPORE, K95
Primary DI / UDI-DI
08055672306136
Basic UDI-DI
805567230KITTTRLF
EMDN Code
T020199, T020401
Device Class
Class I
Medical Purpose
SET PROCEDURARE COMPOSTO DA TELI E CAMICI UTILIZZATI PER ALLESTIRE E MANTENERE IL CAMPO STERILE IN AMBITO CHIRURGICO

Manufacturer details

EUDAMED SRN
IT-PR-000032985

Other devices from So.Ge.Si. S.p.A.

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Properties

  • Sterile