BEUDAMED
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    BARI-KAD PACKING DEVICE

    FDA 510(k)
    FDA Class 1 ·Dental

    SYNCHROMED

    FDA Adverse Event
    Other ·MEDTRONIC, INC., NEUROLOGICAL DIV·Product code LKK·November 24, 2004

    ALLEVYN GENTLE BORDER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW MEDICAL LTD.·Product code NAD·April 7, 2016

    INFUSOMAT SPACE - US VERSION

    FDA Adverse Event
    B. BRAUN MELSUNGEN AG·Product code FRN·November 11, 2013

    ANTI-K (HUMAN MONOCLONAL) SERIES 2

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·December 14, 2007

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 18, 2013

    2.4 THRD RED TOOL SELF-DRILLING 78 HEX-S

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·June 18, 2021

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC.·Product code GEX·December 21, 2018

    ENDURITY MRI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·July 13, 2017

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·March 28, 2024

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code CCK·December 13, 2023

    OLYMPUS-KEYMED

    FDA Adverse Event
    Death ·KEYMED (MEDICAL & INDUSTRIAL EQUIPMENT) LTD.·Product code EZM·October 17, 1997

    BARDIA SILICONE 2-WAY, 5CC FOLEY CATHETER, 14 FR.

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·April 13, 2017

    JETSTREAM XC

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MCW·January 30, 2023

    VIDEO TELESCOPE "ENDOEYE HD II", 5.4 MM, 30°, AUTOCLAVABLE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·June 6, 2024

    MEDFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·February 19, 2020

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·July 19, 2023

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LKK·November 6, 2002

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·June 17, 2024

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC.·Product code GEX·October 20, 2018