BEUDAMED
    27 results · 22ms · Sources: EU EUDAMED, US FDA

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    BRAIN BIOPSY NEEDLE

    FDA 510(k)
    FDA Class 2 ·Neurology

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017712·K-Wire, Double Ended, Trocar Point, Diameter Si...

    75H - Capitol Drywall - 2-Shelf Cabinet

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588120942·75H - Capitol Drywall - 2-Shelf Cabinet

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111241963·WOLF BOEHLER PLASTER CAST BRKR

    Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08809265159681·

    Rod Gripper

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215068783·

    MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CRE¿ WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·February 20, 2013

    CRE¿ WIREGUIDED

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - CORK·Product code KNQ·September 7, 2012

    CRE? WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·June 18, 2013

    CRE¿ WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·January 7, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 2, 2013

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·June 2, 2011

    GPS PROCEDURAL STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FPO·August 6, 2008

    CRE¿ WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·March 13, 2013

    CRE¿ WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·August 10, 2012

    Microtek Franz Angiography Drape with Radiation Shield, Item # RBA202, and Microtek Angiography Drape with Radiation Shield and Pouches, Item # RBA203. Sterile EO. Microtek Medical, Inc., Columbus, MS 39702.

    FDA Enforcement
    Class II ·Terminated·Ecolab Inc·September 14, 2016

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EFB·December 6, 2018

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EFB·December 6, 2018