BEUDAMED
    4 results · 19ms · 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 ×

    SYRINGE 0.3ML 31G 8MM WHOLEUNIT 10BG 500

    FDA Adverse Event
    Injury ·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·March 10, 2026

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 2, 2014

    PORTEX 8.0MM CUFFED TRACHEAL TUBES

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD, INC.·Product code BTR·October 25, 2012

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·September 22, 2010