BEUDAMED
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    CONMED ALTRUS THERMAL TISSUE FUSION SYSTEM

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526189799·LEVAMED ACTIVE ANKLE SUP BLACK R IV

    Medline Industries, Inc.

    FDA UDI
    MEDLINE INDUSTRIES, INC.·10198459280573·TRAY SUTURE

    FINOCHIETTO RETRACTOR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896090767·FINOCHIETTO RETRACTOR LARGE SIZE SPREAD

    EEG MIS MONITOR MODEL # A-2000; BIS ENGINE

    FDA 510(k)
    FDA Class 2 ·Neurology

    PINNACLE ACETABULAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    4WEB Medical

    FDA UDI
    4web Medical·00812998054633·

    4WEB Medical

    FDA UDI
    4web Medical·00812998054619·

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93051015342S30·Long Curette 15" custom REV ANG 90°

    4WEB Medical

    FDA UDI
    4web Medical·00812998054626·

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93051015344S30·Long Curette 15" custom Lateral Left

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93051015343S30·Long Curette 15" custom Lateral Right

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 17, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·December 28, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 12, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·August 9, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 6, 2013

    ACTIVELIFE 1 PC - 1 PC UROSTOMY CONVEX POUCH W/DURAHESIVE (DH)

    FDA Adverse Event
    Injury ·CONVATEC INC.·Product code EXH·August 19, 2014