BEUDAMED
    4 results · 27ms · 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 Status: Other ×

    KENTRON - ADULT PULMONARY RESUSCITATOR

    FDA Adverse Event
    Other ·UNOMEDICAL S.A. DE C.V.·Product code BTM·October 28, 2009

    AMBU SPUR II ADULT RESUSCITATOR

    FDA Adverse Event
    Other ·AMBU INC.·Product code BTM·January 27, 2014

    AMBU SPUR ADULT

    FDA Adverse Event
    Other ·AMBU, INC.·Product code BTM·August 9, 2001

    AMBU SPUR

    FDA Adverse Event
    Other ·AMBU, INC.·Product code BTM·October 10, 2002