BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    LUCENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUILE WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.0.2

    FDA 510(k)
    FDA Class 2 ·Neurology

    CODA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·October 23, 2017

    LCP PROXIMAL LATERAL TIBIA PLATE 11 HOLES/260MM-RIGHT

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·October 1, 2021

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·May 21, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

    LOGICAL SINGLE KIT

    FDA Adverse Event
    Injury ·SMITHS MEDICAL INTL., LTD.·Product code DRS·June 9, 2011

    CODA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·September 10, 2019

    DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·August 10, 2023