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

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    FARRELL VALVE SYSTEM WITH EQUILIBRIUM TECHNOLOGY AND ENFIT ENTERAL CONNECTORS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694026529·MFx Angulated Locking BSSO Plate, 6 Hole, Medium

    Encompass Hip Stem

    FDA UDI
    Ortho Development Corporation·00822409012961·12mm Cement Restrictor

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707010968·CALIBRA 1ST MOL BANDS W/G8025-02 n.UR 12

    DIGITAL RADIOGRAPHY

    FDA 510(k)
    FDA Class 2 ·Radiology

    TEH LIN POWER SCOOTER, MODEL TL-822

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Magna-FX®

    FDA UDI
    Zimmer, Inc.·00889024024731·

    I-STAT PT/INR CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE INC.·Product code GJS·April 3, 2012

    I-STAT PT/INR CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE, INC.·Product code GJS·March 30, 2012

    AMS 800 URINARY CONTROL SYSTEM WITH INHIBIZONE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EZY·December 11, 2018

    PELVICOL ACELLULAR COLLAGEN MATRIX 4X7CM

    FDA Adverse Event
    Injury ·COVIDIENT, FORMERLY TISSUE·Product code FTL·September 17, 2012

    PARIETEX UGYTEX PP POSTERIOR KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·September 17, 2012

    I-STAT PT/INR CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE, INC.·Product code GJS·March 28, 2012

    I-STAT PT/INR CARTRIDGES

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE INC.·Product code GJS·March 26, 2012

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 4, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·June 28, 2011

    LUMAX 540 DR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code MRM·May 17, 2012

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Injury ·OPTONOL, LTD·Product code KYF·April 5, 2012

    PMT INTEGRA TISSUE EXPANDER

    FDA Adverse Event
    Other ·PMT CORP.·Product code LCJ·March 21, 2012