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Bpt Ext + 200

by Phoenix S.R.L.

Ref PR20403157Model Dispositivi per Infusione ed Aspirazione

Active European Union

CE MDR

Valid until

13 Feb 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier ICIM S.P.A.

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 Number0425-MDR-030019-04 Date23 Jul 2026IssuedStatusActive expires 13 Feb 2028

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 0425-MDR-030019-04 Active

    Quality management system EU MDR

    Certifier
    ICIM S.P.A. 0425
    Issued
    23 Jul 2026
    Expires
    13 Feb 2028

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Dispositivi per Infusione ed Aspirazione, PR20403157
Primary DI / UDI-DI
08052747955374
Basic UDI-DI
805274795INFNN
EMDN Code
A03020199 Extensions - other
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000023426

Other devices from Phoenix S.R.L.

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Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No