BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Alteon® HA Femoral Stems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DePuy Corail AMT Hip Prosthesis

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    WatchPAT200U (WP200U)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD LUER-LOK¿ TIP SYRINGE ONLY

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·July 28, 2023

    FLEXIVA (TM) TRACTIP HIGH POWER SINGLE-USE LASER FIBER

    FDA Adverse Event
    Malfunction ·MEDVENTURE TECHNOLOGY CORPORATION·Product code GEX·November 11, 2014

    AUTOCAT 2 WAVE GERMAN

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·August 24, 2011

    RESERVOIR 1.8ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·July 23, 2013

    GMK HINGE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·March 5, 2025