BEUDAMED
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    CAG-02A

    FDA 510(k)
    FDA Class 2 ·Radiology

    Pure Enrichment

    FDA UDI
    BEAR DOWN CONSULTING·00817387028004·

    SCoV-2 Ag Detect™ Rapid Self-Test

    FDA UDI
    INBIOS INTERNATIONAL, INC·B379CAGS21·

    Pure Enrichment

    FDA UDI
    BEAR DOWN CONSULTING·00817387027960·

    CERAMATEC MAXCELL AND CAG GALVANIC OXYGEN SENSORS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BABY-VAC

    FDA Adverse Event
    Malfunction ·CAG INT'L·Product code GCX·November 22, 2000

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·September 30, 2019

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 26, 2020

    ENDEAVOR RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·June 30, 2010

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 26, 2020

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 26, 2020

    LAUNCHER

    FDA Adverse Event
    Injury ·MEDTRONIC, INC·Product code DQY·October 1, 2021

    FARAWAVE PULSED FIELD ABLATION CATHETER, 31MM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code QZI·January 24, 2025

    SYNERGY¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 22, 2017

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·April 19, 2006

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·March 5, 2009

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·March 5, 2009

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·July 28, 2008

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·July 28, 2008

    ENDEAVOR RESOLUTE RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·June 26, 2015