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

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    REVELATION POROUS HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COMBISON(R) 330, MODEL # IR17.5AG/A & VRW177AK/A

    FDA 510(k)
    FDA Class 2 ·Radiology

    B-D PEN NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    2520274-2013-10954

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MQP·February 27, 2013

    MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code LXH·February 16, 2011

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    OSS REINFORCED YOKE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·March 21, 2023

    UNKNOWN PALACOS CEMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·April 11, 2023

    STAINLESS STEEL K-WIRE 1.6MM

    FDA Adverse Event
    Malfunction ·BIOMET TRAUMA·Product code HTY·June 22, 2017

    OSS CEMENTED IM STEM 15X225

    FDA Adverse Event
    Injury ·.·Product code JDI·March 21, 2023