BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    MONSANTO SANTOPRENE (PERITONE DEVICE)

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    JOBST Maternity

    FDA UDI
    BSN MEDICAL, INC.·04042809641530·OPAQUE MATERNITY 20-30 MM HG KNEE HIGH ZIG ZAG ...

    TINA-QUANT MYOGLOBIN GEN.2 TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    SYSTEM 1E Liquid Chemical Sterilant Processing System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ATTAIN ABILITY STRAIGHT

    FDA Adverse Event
    Malfunction ·MPRI·Product code OJX·June 10, 2014

    TRANSVENE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWS·October 8, 2010

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON INC·Product code OTN·December 7, 2012

    PINNACLE 100 ACET CUP 50MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·May 30, 2019

    OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

    FDA Enforcement
    Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012