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Ddk-A/Syr E 22g

by Phoenix S.R.L.

Ref 136000179

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 Number805274795SCANV Basic UDI-DI 08052747958009UDI-DIDate9 Sep 2025RegisteredStatusActive

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  • Withdrawn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
KIT PROCEDURALE CON SIRINGA e AGO
Model / Reference
136000179
Primary DI / UDI-DI
08052747958009
Basic UDI-DI
805274795SCANV
EMDN Code
A0101010102, A020102020102
Device Class
Class IIa
Medical Purpose
Somministrazione al paziente di radiofarmaco.

Manufacturer details

EUDAMED SRN
IT-PR-000046613

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Properties

  • Sterile