BEUDAMED
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    T2 ICF

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    SOUTHERN IMPLANTS (PTY) LTD·06009544035671·Impression Coping Fully Guided RT

    iHealth

    FDA UDI
    IHEALTH LAB INC.·00850044118427·

    iHealth

    FDA UDI
    IHEALTH LAB INC.·00850044118434·

    iHealth

    FDA UDI
    IHEALTH LAB INC.·00850044118458·

    PARAINFLUENZA-I-CF ANTIGEN AND CONTROL ANTIGEN

    FDA 510(k)
    FDA Class 1 ·Microbiology

    INTRACLUDE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DXC·January 16, 2014

    POLIO TYPE I CF ANTIGEN, & TYPE II, III

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PROSIMA PELVIC FLOOR REPAIR KIT

    FDA Adverse Event
    Injury ·ETHICON INC·Product code OTP·October 23, 2012

    INTRACLUDE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DXC·February 6, 2014

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON INC·Product code OTN·October 23, 2012

    INTRACLUDE INTRA-AORTIC OCCLUSION CATHETER

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DXC·February 10, 2020

    CROWN DRILL T2 ICF

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HWE·September 23, 2020

    BD COR GX INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MAQ·February 8, 2023

    BONE PLUG EXTRACTOR T2 ICF

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code LXH·September 23, 2020

    BONE PLUG EXTRACTOR T2 ICF

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code LXH·September 17, 2020

    EXCEL MULTI III

    FDA Adverse Event
    Injury ·EXCEL TECH LTD·Product code GZJ·August 6, 2004

    BACTEC PLASTIC MYCOSIS IC/F MEDIUM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·November 3, 2025

    ENDOPATH ETS COMPACT FLEX45 ENDOSCOPIC ARTICULATING LINEAR CUTTER FOR OPEN PROCE

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·November 7, 2007

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·October 1, 2015