BEUDAMED
    9 results · 35ms · 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 ×

    PANORAMA CENTRAL STATION

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

    GENESIS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·August 28, 2014

    ENDOSTAT ELECTROSURGICAL UNIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code KNS·May 17, 2011

    VARIABLE LOCK SCREW 4.75X35MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWJ·January 24, 2018

    MAESTRO TC CARPALHD 7X15MM STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWN·January 24, 2018

    MAESTRO TC CARPAL PLATE 9X37MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWJ·January 24, 2018

    VARIABLE LOCK SCREW 4.75X15MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWJ·January 24, 2018

    MAESTRO RAD W/BRG 7X15 7.5 RT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWJ·January 24, 2018

    MAESTRO RADIAL STEM 6.0X40MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWJ·October 23, 2017