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

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    RXG DISTRACTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517565389·CoRoent Ant TLIF PEEK, 13x13x30mm 4°

    WESTCOTT TENOTOMY SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896014497·WESTCOTT TENOTOMY SCISSORS CURVED BLUNT MEDIUM ...

    Zavation

    FDA UDI
    Zavation LLC·00197157006075·Sizer with One Stop/6deg/11&12mm

    BLADDER SCANNER

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATION TO DASH 3000/4000 PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAPSUREFIX

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·December 9, 2015

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·May 29, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 20, 2011

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·August 22, 2008

    Welch Allyn Vital Signs Monitor 5300 Series 300 Part numbers 007-0098-00 through 007-0159-00

    FDA Recall
    Terminated ·Welch Allyn Protocol, Inc·Product code DQA·June 8, 2004