BEUDAMED
    68 results · 23ms · Sources: EU EUDAMED, US FDA

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    FLEX-TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    DUFNER Instrumente GmbH

    FDA UDI
    DUFNER - Instrumente GmbH Fabrik ärztlicher Instrumente Medizintechnik·04063763199684·MICTEC Flexible trocar set TITANIUM, Ø7 mm, 70 ...

    TITANIUM MICTEC FLEXIBLE TROCAR SET

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896007802·TITANIUM MICTEC FLEXIBLE TROCAR SET

    TITANIUM MICTEC FLEXIBLE TROCAR SET

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09920907170·TITANIUM MICTEC FLEXIBLE TROCAR SET

    Spliceable Tunneling Sleeve CH12

    FDA UDI
    RAUMEDIC AG·04057834023831·

    SMITH & NEPHEW SUTURELOK, MODEL 7207321

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EBV V VCA IGM ELISA KIT MODEL# EBM-200

    FDA 510(k)
    FDA Class 1 ·Microbiology

    AXXENT FLEXISHIELD MINI (K090417)

    FDA Adverse Event
    Injury ·XOFT, INC.·Product code IXI·January 7, 2011

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 17, 2014

    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

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 2, 2013

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·September 15, 2014

    DRILL BIT FAST 4.0MM SHORT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXT·April 29, 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

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 20, 2014