BEUDAMED
    26 results · 36ms · Sources: EU EUDAMED, US FDA

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    Bact-Trap Filter, Bact-Trap Mini, Bact-Trap Midi, Pharma Mini HME/Filter, Bact-HME HME/Filter and Bact-HME Midi HME/Filter

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112946·CORNEAL TREPHINE BLADE8.25MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112526·BARRON VACUUM TREPHINE 8.25MM

    Blade Scalpel

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113462·SCLEROTOME BLADE #57 (BX/5)

    PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AUROPAL SOLDER M-1

    FDA 510(k)
    FDA Class 2 ·Dental

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973257·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973301·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970041·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970065·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970058·

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·December 16, 2013

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·February 27, 2014

    VITROS CHEMISTRY PRODUCTS SALICYLATE SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code DKJ·October 8, 2008

    ACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·August 5, 2011

    EMERGE?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·July 2, 2013

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·January 13, 2014

    EVIS EXERA III COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·July 23, 2024

    AXIOS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 17, 2024

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·September 8, 2020