BEUDAMED
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    V200 VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    V200 / ESPRIT

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 16, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 28, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 19, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·May 20, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 7, 2021

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 9, 2020

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 21, 2021

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017712·K-Wire, Double Ended, Trocar Point, Diameter Si...

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950030156·MCALLISTER CONNECTIVE TISSUE GRAFT PLACEMENT IN...

    InnoSpire Elegance

    FDA UDI
    RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD·00383730001784·Innospire Elegance Unit Assembly, 220V 60HZ (BRA)

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112472·BARRON VACUUM TREPHINE 7.0MM

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970010·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970027·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172974018·UniTip High Resolution Catheter 10F

    X-SEPT TRANSSEPTAL SHEATH AND TRANSITION CATHETER, MODEL MV-03-09-90, MV-03-10-90, MV-03-11-90, MV-03-09-120, MV-03-10-1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL SE-312

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD PLASTIPAK LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·August 2, 2021

    INTERNAL PADDLES OPTION FOR DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 22, 2013

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·September 19, 2014