BEUDAMED
    29 results · 21ms · Sources: EU EUDAMED, US FDA

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    AMT G-J TUBE

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526159853·PROTECT.ACHI ANKLE SUPPORT GRAY IV

    ACEMST1

    FDA UDI
    ACEM SPA·08050705890088·ACEMST1.1 ARTICULATED ARM w/BATTERY TROLLEY

    Leva® Anterior Interbody System

    FDA UDI
    Spine Wave, Inc.·10840642108248·Plate, 34 mm (W) x 11 mm (H)

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306818493·Light pipe only for breast retractors, size: 180mm

    MEGABEAM/CERALAS REUSEABLE HANDPIECE AND DISPOSABLE TIPS

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

    GIRAFFE AND PANDA WARMERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DONJOY

    FDA UDI
    DJO, LLC·00888912015325·COLD PAD,UNIV,FOAM,S,EH,XL

    CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·December 14, 2012

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·November 1, 2015

    CAIMAN DISP. INSTR. NON ARTICUL.D:5 / 360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·February 18, 2016

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/ 360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·July 22, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·February 27, 2015

    LMA CLASSIC

    FDA Adverse Event
    LMA NORTH AMERICA, NOW PART OF TELEFLEX·Product code CAE·May 1, 2013

    OXF ANAT BRG LT MD SIZE 4 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·September 23, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 1, 2011