BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    HALYARD® ONE-STEP® Sterilization Wrap, HALYARD® QUICK CHECK® Sterilization Wrap, HALYARD® SEQUENTIAL Sterilization Wrap and HALYARD® SMART-FOLD® Sterilization Wrap

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Pomee

    FDA UDI
    POMEE CORPORATION·G15772340500·4 3/4" angled with 1 serrated blade

    Spud

    FDA UDI
    KATENA PRODUCTS, INC.·00841668101216·FRANCIS FOREIGN BODY SPUD

    J & J INSTRUMENTS

    FDA UDI
    J & J INSTRUMENTS INC·00817524025828·WIRE CUTTING SCI 4.75"" ANG

    ENT Nasopharyngoscope and Accessories

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD NEXIVA 22 GA X 1.00IN SP WITH MAXZERO

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·January 6, 2024

    BD NEXIVA 20 GA X 1.00IN SP WITH MAXZERO

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·January 5, 2024

    EXTRACTOR XL TRIPLE LUMEN RETRIEVAL BALLOON

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GCA·November 4, 2008

    TRIATHLON P/A CR BEADED #5R

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code MBH·August 29, 2011

    CORE UNIVERSAL DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·July 18, 2013

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·November 19, 2018