BEUDAMED
    11 results · 29ms · Sources: EU EUDAMED, US FDA

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    CONSEAL(TM) COLOSTOMY CONTINENCE SYSTEM

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111390·MICRO NEEDLE HOLDER CURVED TITANIUM

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108437·KATENA NEEDLE HOLDER CURVED

    REMSTAR AFLEX CPAP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    3-DAY BIOINDICATOR RELEASE PROCESS FOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TC3 RP TIBIAL INSERT S5,12.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code NJL·June 10, 2014

    ATW MARKER GUIDEWIRE

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code DQX·October 11, 2010

    INTERSTIM II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code EZW·December 10, 2012

    G7 NEU +5MM E1 LINER 36MM F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 7, 2021

    FEMORAL STEM PRESS-FIT COLLARLESS 12/14 NECK TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·September 7, 2021

    BIOLOX OPTION, HEAD, L, 36/+3.5, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LZO·August 23, 2021