BEUDAMED
    58 results · 22ms · Sources: EU EUDAMED, US FDA

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    HYPROCURE SUBTALAR IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Leksell Stereotactic System

    FDA UDI
    Elekta Instrument AB·07340048300926·MR-ADAPTER PICKER EDGE

    AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 30mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665010176·

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867522510·Cannulated Canc Screw, FT, 7.0x30mm

    Implant-One

    FDA UDI
    Implant Logistics, Inc.·D762APT0420300·Abutment, 400 Series Angled Post 2mm Cuff Heigh...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420420320·Anterio Lateral Closing Wedge Osteotomy Guide, ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710400420300·Anterior Dome Osteotomy Guide, 42mm x 30mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710410420300·Anterior Closing Wedge Osteotomy Guide, 42mm x ...

    C & B FORMULA

    FDA UDI
    AMERICAN TOOTH INDUSTRIES·D772ATI400420300·C & B FORMULA 1 LB SHADE 30

    PORTABLE INTENSIVE CARE UNIT

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    OMNI-TRAK 3150/3155A SERIES MONITOR WITH ANESTHETIC AGENT, MODEL 3155A SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    36MM COCR BIOMET FEM HD STD NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 13, 2016

    UNKNOWN EXCEED HIP

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

    UNKNOWN RECAP 48MM HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·September 16, 2016

    36MM 12/14 TPR FEM HEAD -4 NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 28, 2016

    EXCEED ABT M2A-36 MOD HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 28, 2016

    EXCEED ABT RINGLOC-X SHELL

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·July 20, 2017

    M2A MOD HD COCR DIA28/+3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·December 23, 2015

    32MM COCR BIOMET FEM HD STD NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·February 16, 2016

    RECAP/MAGNUM ACETABULAR SHELL

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·February 15, 2017