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ASTER KIT (Hc=49) CE

by Phoenix S.R.L.

Ref 141000021

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805274795KABMH Basic UDI-DI 08052747959624UDI-DIDate8 Jan 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  • Withdrawn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

Device Name
PPF002 - Kit Aster
Model / Reference
141000021
Primary DI / UDI-DI
08052747959624
Basic UDI-DI
805274795KABMH
EMDN Code
A03010101, A03010105
Device Class
Class IIa
Medical Purpose
Prelievo da contenitore e somministrazione al paziente di farmaco radiometabolico

Manufacturer details

EUDAMED SRN
IT-PR-000046613

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Properties

  • Sterile