BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    GENESYS PRESSFT SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Arthrex

    FDA UDI
    Provision·B504OMAR1218900·

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867087873·DRILL, 9MM CANNULATED

    Reprocessed 9mm Cannulated Drill Bit

    FDA UDI
    SURETEK MEDICAL·B390AR1218901·

    G-2 VERSION 3, MODEL 10049

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BALL ABUTMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·April 29, 2014

    CONTOUR

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·April 5, 2019

    EXCLAIM 8

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 15, 2013

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code JTC·June 12, 2008

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·June 9, 2011

    G7 SCREW 6.5MM X 25MM

    FDA Adverse Event
    Death ·ZIMMER BIOMET, INC.·Product code LPH·August 6, 2021

    G7 SCREW 6.5MM X 25MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 6, 2021

    ACCESS ACCUTNI REAGENT

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code MMI·September 15, 2016