BEUDAMED
    9,209 results · 24ms · Sources: EU EUDAMED, US FDA

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    SHARPS CADDY MAGNETIC & SHARPS CADDY FOA

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Macintosh FO (A) Detachable Blade

    FDA UDI
    Maco International·G272FO431350·

    Macintosh FO (A) Detachable Blade

    FDA UDI
    Maco International·G272FO43120·

    Macintosh FO (A) Detachable Blade

    FDA UDI
    Maco International·G272FO43140·

    Macintosh FO (A) Detachable Blade

    FDA UDI
    Maco International·G272FO43110·

    Macintosh FO (A) Detachable Blade

    FDA UDI
    Maco International·G272FO43130·

    GUIDANT 4.5 MM HEARTSTRING PROXIMAL SEAL

    FDA Adverse Event
    Malfunction ·GUIDANT CARDIAC SURGERY·Product code DXC·June 26, 2005

    ELECTRODE, ECG, MONITORING, SS SNAP, FOA

    FDA Adverse Event
    Malfunction ·INTCO MEDICAL CO.·Product code DRX·December 14, 2015

    FIBEROPTIX ULTRA 8 IAB: 8FR 40CC

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DSP·January 28, 2019

    RESOLUTION CLIP DEVICE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code GDO·April 12, 2006

    VERITY DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 15, 2014

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·April 14, 2014

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·February 20, 2014

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·March 7, 2014

    LECTROVAC 6-INCH

    FDA Adverse Event
    Malfunction ·VALLEYLAB·Product code GEI·August 14, 2007

    WAVELIGHT FS200 FEMTOSECOND LASER

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code OOE·April 6, 2015

    SENSATION PLUS 8FR. 50CC IAB & ACCESSORIES (W/PRESSURE TUBES, NO STYLET)

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·October 6, 2025

    C-TAPER COCR LFIT HEAD 40MM/+10

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·June 21, 2012

    UNKNOWN DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 22, 2008

    NEWTON IQ W/STAY SAFE CYCLER SET

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code KDJ·February 11, 2014