BEUDAMED
    11 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    DYNAMIK INTERVERTEBRAL BODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNICORN MODEL SYS0630

    FDA 510(k)
    FDA Class 2 ·Radiology

    PRESSURE ACTIVATED CHECK VALVE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 8, 2024

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·Product code KWP·November 2, 2021

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·Product code KWP·November 2, 2021

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·Product code KWP·November 2, 2021

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FPA·April 29, 2013

    32MM MOD HD COCR -6MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·September 11, 2014

    ENDOPATH XCEL BLADELESS TROCAR WITH STABILITY SLEEVE, 11MM DIAMETER - 100 MM LEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GCJ·July 22, 2008

    G7 10 DEG ARCOMXL LINER 36MM E

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·December 27, 2017