BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

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    V-CATH POLY PICC

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRUEBLUE

    FDA UDI
    Respironics, Inc.·00606959004528·RP TRUEBLUE HEADGEAR

    Tiche PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481476491·

    DIAMEDIX IS-RUBELLA IGM CAPTURE TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MODIFICATION TO THE TAC' PIN

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD INSYTE¿ AUTOGUARD¿ WINGED SHIELDED IV CATHETER 18GA 1.16IN (1.3 X 30 MM)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·January 3, 2020

    COMPRESSION FORCEPS

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTD·April 22, 2013

    AP STANDARD RAPID-PORT EZ

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·August 12, 2014

    ARCHITECT I1000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·April 28, 2011

    NIBP CUFFS

    FDA Adverse Event
    Injury ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code OED·August 8, 2025