BEUDAMED
    11 results · 24ms · Sources: EU EUDAMED, US FDA

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    CORVAC PLASTIC BLOOD COLLECTION TUBE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SwishActive™ Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307106746·Ø3.7 x 8 Platform 3.5mmD

    BIOPORE 493-05 ENDOCARDIAL IMPLANTABLE PACING LEAD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GLYC-AFFIN GP

    FDA 510(k)
    FDA Class 2 ·Hematology

    GYNECARE TVT OBTURATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code OTN·October 29, 2024

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·December 10, 2010

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·February 5, 2013

    MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 18, 2014

    GYNECARE TVT OBTURATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code OTN·September 16, 2024

    SINGLE USE PAPER FILTER WITH INDICATOR

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code FRG·January 30, 2019

    TM-ECOCHGTRODE

    FDA Adverse Event
    Other ·NATUS MEDICAL INC·Product code GXY·January 9, 2009