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

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    G3 Active Plate Large Fragment System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·March 31, 2016

    ACQPOINT THERMAJADE MASSAGE TABLE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    GAMBRO PRISMAFLEX HF1000 AND HF1400 SETS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BMT GB KNEE STM 12X40

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OIY·June 1, 2022

    PRISMAFLEX SETS (HF)

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORPORATION·Product code KDI·May 22, 2023

    ABS FIXATION DEVICE W/15 TACKS

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·October 6, 2014

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 9.75CM

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·May 30, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 20, 2011

    ProScreen 6 Panel Dip Card, Item No. PSCuPSD-6BUP300, PSD-6MTDBO300, PSD-6BUPO, PSD-6MBO, PSD-6MB,

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015