BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    HEXAPOLAR ELECTRODE BALLOON FLOTATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERIFY Assert VH2O2 Self-Contained Biological Indicator

    FDA 510(k)
    FDA Class 2 ·General Hospital

    STETHOSCOPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNCHRON® ALT REAGENT, 2 X 200 TEST

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CKA·July 26, 2011

    QC F/K-WIRES Ø0.6-3.2 F/532.001 532.010

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code HWE·July 10, 2017

    PHYSIOMESH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·February 21, 2013

    CVC SET: 16 GA X 16 CM

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL INC·Product code DQY·January 21, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 31, 2014