BEUDAMED
    56 results · 33ms · Sources: EU EUDAMED, US FDA

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    SYNTHES (USA) STERILE STERNAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EASYLIFE

    FDA UDI
    Respironics, Inc.·00606959027848·EasyLife Mask w/Headgear, Small, Japan

    Copper Ni-Ti - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989025453·COPPER NITI 27 BAF 14 DIA U/L PK10

    OptiLIF Endo, Direct Visualization System

    FDA UDI
    SPINEOLOGY INC.·M7401050041·TF Endo Tubular Retractor, 7.5mm x 163mm x 40° ...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450333747·

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0100410·Caddie Lid, Curved Rods

    NA

    FDA UDI
    ZIMMER TRABECULAR METAL TECHNOLOGY INC.·00889024311459·

    SLT DIFFUSER FIBER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    IALUSET HYDROCOLLOID

    FDA 510(k)
    FDA Unclassified ·Unknown

    PRIMORIS HIP STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 5, 2016

    PRIMORIS FEMORAL STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·October 3, 2017

    PRIMORIS NECK PROSTH BM SZ 26

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 4, 2016

    PRIMORIS HIP STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 5, 2016

    MARY HITCHCOCK HANOVER NH 1

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·November 7, 2012

    PRMRS NCK STEM TI BM SZ 24 RSA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·June 23, 2016

    TAPERLOC LAT COCR 10MM T1

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 20, 2026

    TPRLOC COCR CMTD STEM T1 7.5MM

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 20, 2026

    UNKNOWN PRIMORIS HIP

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 4, 2016

    PRMRS NCK STEM TI BM SZ 24 RSA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWY·April 13, 2018

    HEM-O-LOK MEDIUM-LARGE CLIP APPLIER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·April 10, 2013