BEUDAMED
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    POLAMEDCO TRACHEAL AND NASOTRACHEAL TUBES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PAQ.209X150X200.AR2100

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763009313·

    Stryker Universal Select Sterilization Tray System

    FDA UDI
    PARAGON MEDICAL, INC.·00857387006268·2.0 MP Screw Module

    I-STAT PT CONTROL LEVIEL 1 I-STAT PT CONTROL LEVEL 2

    FDA 510(k)
    FDA Class 2 ·Hematology

    DEVILBISS MODEL 9200D HEATED HUMIDIFIER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DATASCOPE PERCOR STAT DL 9.5 FR 40CC

    FDA Adverse Event
    Malfunction ·DATASCOPE·Product code DSP·March 18, 1992

    TOTALCARE BARIATRIC

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 6, 2010

    FORTIFY VR, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 8, 2014

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 26, 2012

    PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS TRACHEOSTOMY TUBE 7.0MM TIGHT TO SHAFT CUFF, Product Code/List Number/Item Code 670170; b) TTS TRACHEOSTOMY TUBE 8.0MM TIGHT TO SHAFT CUFF 1/EA, Product Code/List Number/Item Code 670180

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·September 4, 2024