BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    INTESTINAL SPONGES

    FDA 510(k)
    FDA Unclassified ·Unknown

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867386488·Cortical Screw, 2.7 mm x 10 mm

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867046733·LO-PRO SCRW TM SS 2.7MMX 10MMCORTEX

    Fetal Doppler, Model FD88

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

    SAFECHILD ENTERAL FEEDING TUBE AND ACCESSORIES AND FEEDING TUBE EXTENSION SET

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

    SYMBIQ SCHANNEL 3.01

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 10, 2014

    EON MINI 16-CHANNEL IPG

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·October 13, 2010

    BALANCED SALT SOLUTION

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL OPTICS·Product code KYB·December 20, 2012

    Breast Pack, part number AMS3238(A Breast Pack, part number AMS4419(A Breast Pack, part number AMS4419(B Breast Pack, part number AMS5750 Breast Pack, part number AMS5750(A Breast Pack, part number AMS6120 Breast Pack, part number PSS1784(B Breast Pack, part number PSS2272(A

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017