BEUDAMED
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    VITAL SIGNS MONITOR MODEL M3B

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Medline Industries, Inc.

    FDA UDI
    MEDLINE INDUSTRIES, INC.·10198459282201·TRAY LAVAGE EDLICH GASTRIC

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111346460·PITCHER/BEAKER W/HANDLE 2000ML

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383501644·Gutta Percha Points is used to root canal filin...

    Sklar

    FDA UDI
    SKLAR CORPORATION·50649111296176·PITCHER W/HAND 2000ML CS/6

    Sklar

    FDA UDI
    SKLAR CORPORATION·30649111260388·PITCHER BEAKER W/HANDLE PK/12

    RENU MULTIPLUS MULTI-PURPOSE SOLUTION

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ROSSMAX MEDIPRO MODEL 100, MODEL 200, AND MODEL 300 BLOOD PRESSURE MONITORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973646·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973561·

    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

    6000 CMS IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 30, 2013

    S4S/SUR-FIT NATURA 2 PC- 2 PC DURAHESIVE (DH) FLEXIBLE WAFER

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

    INRATIO

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code GJS·May 20, 2011

    S4S/SUR-FIT NATURA 2 PC - 2 PC DURAHESIVE (DH)

    FDA Adverse Event
    Injury ·CONVATEC DOM. REPUBLIC, INC.·Product code EXE·August 14, 2014