BEUDAMED
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    GA-I

    FDA UDI
    AGNES MEDICAL CO., LTD.·08800067700033·

    FLOWFLEX COVID-19 ANTIGEN HOME TEST

    FDA Adverse Event
    Malfunction ·ACON LABORATORIES, INC.·Product code QKP·February 6, 2023

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code NIQ·October 13, 2017

    AUTO SUTURE MULTIFIRE GAI 60-3.8

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP·Product code GAG·October 20, 1997

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·October 13, 2017

    SWAN- LOCK SWABABLE 2 GANG 4 WAY HIGH FLOW STOPCOCK

    FDA Adverse Event
    Injury ·CODAN US CORP.·Product code FPA·April 30, 2025

    AUTO SUTURE ENDO-GAI MULTIIRE 30-2.5

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·October 9, 1996

    GA-B, GA-C, GA-E, GA-I, GA-S, GA-W3A, GA-F3A, GA-IL, GA-SL, GA-W3B, GA-F1A

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AUTO SUTURE MULTIFIRE ENDO GAI II 45-3.5 DLU

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·June 29, 1999

    CUSTOM MADE DEVICE GAI LEFT PM-TMJ & MODEL

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·July 3, 2018

    PIPELINE

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 20, 2019

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·November 7, 2019

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·June 11, 2019

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 5, 2017

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·August 4, 2023

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 1, 2019

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·December 5, 2019

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·July 23, 2019

    PILLING ASPIRATING NEEDLE 23GA

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GAI·June 16, 2010

    NABATOFF VEIN STRIPPER SET

    FDA Adverse Event
    Injury ·AESCULAP, INC.·Product code GAI·May 7, 2007