BEUDAMED
    47 results · 31ms · Sources: EU EUDAMED, US FDA

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    NEV'S INK AUTOCLAVE TAPES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BETA/Pak

    FDA UDI
    Bio/Data Corporation·G0561015801·

    ZAVATION TAP

    FDA UDI
    Zavation LLC·00197157013288·TIGER 2 TAP, Ø 8.0mm, EXCELSIUSGPS CANNULATED

    SIMPLICITY SOFT QD SILVER INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GROSS FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·February 22, 2026

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 1, 2013

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 19, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 11, 2011

    EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FAD·March 12, 2015

    CAPSUREFIX NOVUS MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 27, 2024

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·May 1, 2018

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MUM·November 16, 2017

    EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·November 12, 2014