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

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    MAGNETOM Avanto Fit

    FDA 510(k)
    FDA Class 2 ·Radiology

    BIOMET MODULAR FEMORAL REVISION SYSTEM

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    TILOCK PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

    (END) SCREW EXTENDER SLEEVE

    FDA Adverse Event
    Malfunction ·ABBOTT SPINE·Product code KWP·October 6, 2008

    F6 DIALYZER FINISHED ASSY (CASE)

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING·Product code FJI·June 24, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011

    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

    ARCOS CON SZ C STD 60MM HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 18, 2019