BEUDAMED
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    DERMASOF

    FDA UDI
    Biodermis LLC·00852260000968·DermaSof Silicone Stick 4.25g tube.

    TEAR DRO

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HSB·August 13, 2018

    AccuBoost®

    FDA UDI
    ADVANCED RADIATION THERAPY, LLC·00850306007179·Shielded Breast Applicator - Round DRO 8cm

    AccuBoost®

    FDA UDI
    ADVANCED RADIATION THERAPY, LLC·00850306007155·Shielded Breast Applicator - Round DRO 6cm

    AccuBoost®

    FDA UDI
    ADVANCED RADIATION THERAPY, LLC·00850306007148·Shielded Breast Applicator - Round DRO 5cm

    AccuBoost®

    FDA UDI
    ADVANCED RADIATION THERAPY, LLC·00850306007162·Shielded Breast Applicator - Round DRO 7cm

    AccuBoost®

    FDA UDI
    ADVANCED RADIATION THERAPY, LLC·00850306007483·Shielded Breast Applicator - 8cm Round DRO Bottom

    AccuBoost®

    FDA UDI
    ADVANCED RADIATION THERAPY, LLC·00850306007476·Shielded Breast Applicator - 7cm Round DRO Bottom

    AccuBoost®

    FDA UDI
    ADVANCED RADIATION THERAPY, LLC·00850306007452·Shielded Breast Applicator - 5cm Round DRO Bottom

    AccuBoost®

    FDA UDI
    ADVANCED RADIATION THERAPY, LLC·00850306007469·Shielded Breast Applicator - 6cm Round DRO Bottom

    SENSATION PLUS 8FR. 50CC DILATOR/SHEATH

    FDA Adverse Event
    Injury ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·May 10, 2023

    PROPAQ MD DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 4, 2016

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 23, 2016

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 17, 2017

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 8, 2016

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 7, 2017

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 12, 2018

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 26, 2018

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 5, 2019

    PROPAQ MD DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 5, 2019