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Buret-Pro

by Pro-Active S.R.L.

Ref BFB000AA180Model BURET-PRO

Active European Union

CE MDR

Valid until

27 Sep 2031

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803402827BFPH Basic UDI-DI 18034028271721UDI-DIDate8 Oct 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 0425-MDR-030220-00 Active

    Quality assurance EU MDR

    Certifier
    ICIM S.P.A. 0425
    Issued
    28 Sep 2026
    Expires
    27 Sep 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
BURET-PRO, BFB000AA180
Primary DI / UDI-DI
18034028271721
Basic UDI-DI
803402827BFPH
Unit of Use DI
08034028271724
EMDN Code
A03010104 Infusion micro-controllers
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
IT-MF-000028985

Other devices from Pro-Active S.R.L.

  • Infu-Pro

    Class I

  • 3-Way Pro

    Class I

  • Uro-Pro

    Class I

  • Pro-Long Tube

    Class I

  • Pro-Omnia Lock

    Class I

  • Pro-Omnia Lock

    Class I

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