BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    Bioflux Software

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bowman Lacrimal Probe

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896120389·Bowman Lacrimal Probe Size 6/7 Butterfly Handle...

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 24, 2025

    XL EXTRACTION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LONGPORT EPISCAN, MODEL-I-200

    FDA 510(k)
    FDA Class 2 ·Radiology

    QUADRA-H CEMENTLESS, HA COATED STEM SIZE 4 LAT

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code JDI·December 30, 2016

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·October 10, 2014

    GYNECARE TVT OBTURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·June 11, 2013

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 14, 2011

    EVOLUTION® ESOPHAGEAL CONTROLLED-RELEASE STENT - PARTIALLY COVERED

    FDA Adverse Event
    Death ·COOK IRELAND LTD·Product code ESW·December 31, 2019

    MALIBU

    FDA Adverse Event
    Injury ·SEASPINE INC.·Product code NKB·February 12, 2020

    MALIBU

    FDA Adverse Event
    Injury ·SEASPINE INC.·Product code NKB·February 12, 2020