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

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    COMET ANTERIOR CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NGB-010 Needle-guided Bracket

    FDA UDI
    Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904001678·

    RHIGENE MESACUP2 TEST- SSB

    FDA 510(k)
    FDA Class 2 ·Immunology

    BPFONE, MODEL UA 767IT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARCOS 18X150MM SPL TPR DIST HA

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 7, 2016

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY 60MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 7, 2016

    ARCOS HA MODULAR REVISION SYSTEM STRAIGHT TAPERED SPLINED DISTAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 10, 2017

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY / TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 10, 2017

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER-SILICON VALLEY·Product code GEX·April 26, 2011

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 2, 2013

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 15, 2014

    ARCOS DISTAL SCREW TI DIA5X50MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·October 12, 2016

    ARCOS DISTAL SCREW TI DIA5X45MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·October 12, 2016

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY TYPE 1 TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 14, 2017

    ARCOS MODULAR REVISION HIP

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code KWA·February 16, 2017

    ARCOS STS DISTAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 23, 2017

    ARCOS MODULAR REVISION HIP SYSTEM STANDARD BROACH PROXIMAL BODY

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·January 6, 2017

    ARCOS CON SZ A STD 50MM HA 0MM SZ A

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 26, 2021

    ARCOS CONE STANDARD BODY FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 24, 2017

    ARCOS HA MODULAR REVISION SYSTEM STRAIGHT TAPERED SPLINED DISTAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 13, 2017