BEUDAMED
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    AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    TOSCA Open end nurse call cable

    FDA UDI
    Radiometer Basel AG·05700693096254·TOSCA Open end nurse call cable

    Troposphere

    FDA UDI
    HENRY SCHEIN, INC.·H65810001171·Troposphere Powder Fine Cut

    e-vive NMES System; Large/XL, Left

    FDA UDI
    Motive Health, Inc.·00854816006912·e-vive NMES System; Large/XL, Left

    CURE 2.0 ACP

    FDA UDI
    SpineArt SA·07640375230829·CERVICAL 1 LEVEL TEMPLATE L17

    CURE 2.0 ACP

    FDA UDI
    SpineArt SA·07640375232212·ANTERIOR CERVICAL PLATE, 1 LEVEL L17

    PARSET SECONDARY ADMINISTRATION SET, LUERLOCK, MODEL A14001E, PARSET SECONDARY SECONDARY ADMINISTRATION SET, MODEL A1400

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACUCAM CONCEPT IV, MODELS A1222B, A1223B, A1221B, A1121B, A1222C, A10402, A10403, A10401

    FDA 510(k)
    FDA Class 1 ·Dental

    SHILEY FENESTRATED LOW PRESSURE CUFFED TRACHEOSTOMY TUBE.

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL, INC.·Product code BTO·September 26, 2000

    SHILEY FENESTRATED LOW PRESSURE CUFFED TRACHEOSTOMY TUBE.

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL, INC.·Product code BTO·September 26, 2000

    SOFLEX SILICONE SQUARE EDGE IOL

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQL·December 16, 2010

    ACCUTORR PLUS NON INVASIVE BLOOD PRESSURE MONITOR (0998-00-0117-XX)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCUTORR PLUS NON INVASIVE BLOOD PRESSURE MONITOR, MODEL # 0998-00-0117-XX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·October 7, 2025

    HUDSON ET TUBE,CF,6.5

    FDA Adverse Event
    Injury ·Product code BTR·November 2, 2021

    MEGASUTURECUT NEEDLEDRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code NAY·March 8, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·February 18, 2011

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·February 19, 2008

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·January 22, 2021

    STERILE 3.0 SOFT KOH-EFF

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HEW·February 20, 2019