BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    NITRILE PATIENT EXAMINATION GLOVES, POWDERED, NON-STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ROUND FILTERS W/INDICATOR

    FDA Adverse Event
    Malfunction ·SPS MEDICAL·Product code FRG·February 28, 2014

    Q3 Distal Access Catheter, Q4 Distal Access Catheter, Q5 Distal Access Catheter, Q6Distal Access Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WRIST TYPE BLOOD PRESSURE MONITOR, HMBPM-005/KINETIK BRANDED BPM2 SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PERMACOL 10X15 1.5MM

    FDA Adverse Event
    Death ·COVIDIEN, FORMERLY TISSUE SCIENCE LABORATORIES, PLC·Product code FTL·September 3, 2013

    FULL-SIZE LID W/RETENTION PLATE SILVER

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code FRG·March 10, 2016

    ACCLAIM ELBOW PIN ASSEMBLY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDC·March 7, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    ATTAIN HYBRID ADJUSTABLE SLITTER

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DRB·August 8, 2014