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Prontoiniezione Ultrafin

by Pikdare S.p.A. 2 variants

Ref 02022982500000

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 Number805809022982500M7 Basic UDI-DI 08058090049166UDI-DIDate2 Jul 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  • Withdrawn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
02022982500000
Primary DI / UDI-DI
08058090049166
Basic UDI-DI
805809022982500M7
EMDN Code
A020199 Syringes, single-use - other
Device Class
Class IIa
Medical Purpose
iniezione e prelievo

Manufacturer details

EUDAMED SRN
IT-PR-000012297

Other devices from Pikdare S.p.A.

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Properties

  • Sterile