BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    BD PLASTIPAK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 1, 2018

    PHYSICA

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code JWH·March 16, 2026

    ACCESS® ACCUTNI

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code MMI·May 8, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·October 17, 2012

    TALENT THORACIC STENT GRAFT SYSTEM - XCELERANT

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·August 11, 2010

    VIDAS® HS TROPONIN I

    FDA Adverse Event
    Injury ·BIOMERIEUX SA·Product code MMI·May 10, 2017

    VIDAS® HS TROPONIN I

    FDA Adverse Event
    Injury ·BIOMERIEUX SA·Product code MMI·May 10, 2017