BEUDAMED
    301 results · 28ms · Sources: EU EUDAMED, US FDA

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    Biomet Headless Compression and Twist-off Screws

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    T7 DRIVER CANN AO

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code LXH·July 14, 2016

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583025094·BL80 NR, PS MAC BLISS 80

    GEN4 INTERACTIVE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828149785·GEN4 INTERACTIVE

    MINISPACER DUAL-SPRAY MDI ADAPTER WITH 22MM (OR 15MM) OD / 22MM OD/ID CONNECTIONS / 15MM ID CONNECTIONS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PROCERA ABUTMENT BRANEMARK, MODELS 10-4001, 10-4004, 10-5001, 10-5004, 10-6001, 10-6004

    FDA 510(k)
    FDA Class 2 ·Dental

    ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·July 14, 2020

    ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·October 30, 2018

    ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·January 5, 2018

    ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·February 28, 2018

    ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·April 30, 2018

    FCG KIT, NEEDLE, BIOPSY

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·April 7, 2020

    FCG KIT, NEEDLE, BIOPSY

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·April 6, 2020

    ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·December 11, 2019

    ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·August 2, 2019

    UNKNOWN DEPUY ACETABULAR SHELL

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JDI·June 3, 2013

    PLUM XLD SPANISH

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·September 26, 2014

    VERITAS COLLAGEN MATRIX-BIOLOGICAL IMPLANT

    FDA Adverse Event
    SYNOVIS SURGICAL INNOVATIONS·Product code FTM·June 16, 2011

    ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·April 15, 2022

    ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·January 15, 2018