BEUDAMED
    14 results · 20ms · Sources: EU EUDAMED, US FDA

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    TRYPTICASE SOY BROTH BLOOD CULTURE BOTT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    BROWNE METREX 1.8% GLUTARALDEHYDE INDICATOR FOR METRICIDE 28 AND METRICIDE PLUS 30 SOLUTIONS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BANTAM CATHETER (280MM BALLOON LENGTHS)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BRILLIANCE 64

    FDA Adverse Event
    PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.·Product code JAK·May 6, 2014

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·October 31, 2012

    GROSHONG NXT CLEARVUE 4 FR SL PICC NURSING FULL TRAY

    FDA Adverse Event
    Injury ·C. R. BARD INC. (BASD)·Product code LJS·August 17, 2010

    MENTOR CPX4 WITH SUTURE TABS, TALL HEIGHT, SMOOTH

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·October 24, 2019

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·May 14, 2020

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·April 8, 2025

    MENTOR CPX4 WITH SUTURE TABS, MED HEIGHT, SMOOTH

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·January 10, 2020

    CPX4 PLUS SMOOTH TALL HEIGHT 550CC

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·April 19, 2022

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·May 14, 2020

    CPX4 WITH SUTURE TABS MEDIUM HEIGHT SMOOTH EXPANDER

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·February 22, 2021

    Karma Flexx Wheelchair Manual Wheelchair.

    FDA Recall
    Terminated ·Karman Healthcare Inc·Product code IOR·January 27, 2016