BEUDAMED
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    DISPOSABLE BLOOD PRESSURE TRANSDUCER DOM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OptiLux LED Illuminator

    FDA UDI
    Medical Illumination International Inc.·00816835024230·LED Illuminator, w/ Mobile Floor Stand, Domestic

    OptiLux LED Illuminator

    FDA UDI
    Medical Illumination International Inc.·00816835024216·LED Illuminator, Portable, Domestic

    ALICE PDX Assembly, DOM

    FDA UDI
    Respironics, Inc.·00606959060388·Alice PDx Portable Sleep Diagnostic System, Dom...

    Lumenis Pulse, Moses 2.0 (DOM)

    FDA UDI
    LUMENIS LTD.·07290109147185·

    Lumenis Pulse 120H

    FDA UDI
    LUMENIS LTD.·07290109145525·

    LEADWIRES,ECG SNAP,DOM,5L,50"

    FDA UDI
    Datascope Corp.·10607567104577·LEADWIRES,ECG SNAP,DOM,5L,50"

    CABLE,ECG PATIENT,DOM,5L,10'

    FDA UDI
    Datascope Corp.·10607567104560·CABLE,ECG PATIENT,DOM,5L,10'

    CLINICAL CHEMISTRY MAGNESIUM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JGJ·January 15, 2019

    ARCHITECT FREE T3

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code CDP·November 5, 2018

    ARCHITECT ESTRADIOL

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code CHP·February 22, 2019

    ACTIVATED ALANINE AMINOTRANSFERASE

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code CKA·June 24, 2021

    BiPAP ST, C SERIES, FLOW GEN, DOM

    FDA UDI
    Respironics, Inc.·00606959043961·BiPAP AVAPS C-Series Domestica FGD SA

    BiPAP AVAPS, C SERIES, FLOW GEN, DOM

    FDA UDI
    Respironics, Inc.·00606959043985·BiPAP AVAPS C-Series Domestica FGD SA

    LDWR,ECG ESIS PINCH,DOM,5L,50"

    FDA UDI
    Datascope Corp.·10607567104706·LDWR,ECG ESIS PINCH,DOM,5L,50"

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·March 12, 2013

    AXIUM DETACHABLE COIL

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code HCG·October 31, 2013

    CPAP PHILLIPS RESPIRONICS SYSTEM ONE HTD HUMID

    FDA Adverse Event
    Injury ·PHILIPS / RESPIRONICS, INC.·Product code MNS·August 4, 2021

    NEXUS AND NXT DETACHABLE COIL

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code HCG·April 21, 2009

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·March 5, 2013