BEUDAMED
    5 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 ×

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·April 30, 2014

    2.7MM LCP(TM) CONDYLAR PLATE 7 HOLES SHAFT

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·February 5, 2013

    PUMP IN STYLE ADVANCED

    FDA Adverse Event
    Other ·MEDELA, INC.·Product code HGX·December 3, 2010

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·April 21, 2025

    UNKNOWN BONE CEMENT

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 3015516266·Product code LOD·April 21, 2025