BEUDAMED
    26 results · 24ms · Sources: EU EUDAMED, US FDA

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    Digital Automatic Blood Pressure Monitor MD3600

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AXIS PACS, HMS PACS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACL TOP

    FDA 510(k)
    FDA Class 2 ·Hematology

    OSSEOTITE® IMPLANT 3.75 X 13MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·December 13, 2019

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 25, 2025

    TI LOW PROFILE SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 25, 2017

    TI LOW PROFILE SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 25, 2017

    EXTRACTOR HANDLE OMEGA2 HANSSON TWIN HOOK

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·June 1, 2011

    M2A-T M/H RAD 2HL SHL 37/48MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 6, 2019

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 11, 2013

    FOUNDATION SHOULDER

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code KWS·June 15, 2011

    AUTODISC 100 TEST STRIPS

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC.·Product code NBW·September 9, 2008

    M2A TPR HI CARBON 37/28MM LNR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 6, 2019

    M2A HI CARBON TAPER LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·February 14, 2017

    M2A HI CARBON MODULAR HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·February 14, 2017

    M2A TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·April 18, 2018

    BI METRIC/XR LAT RPP C/L 10MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 18, 2018

    BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·February 26, 2024

    BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·December 21, 2023

    BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·December 21, 2023