BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    MALE LATEX CONDOM 56MM

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

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197805·AK3 PS-C Insert Trial Size 3, 12mm

    SCIMED 7FR AND 8FR TRIGUIDE GUIDING CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RHEUMAGEN CRP T-CONTROL

    FDA 510(k)
    FDA Class 2 ·Immunology

    TORNIER AEQUALIS REVERSE SHOLDER PROSTHESIS

    FDA Adverse Event
    Malfunction ·TORNIER INC.·Product code HSD·June 18, 2009

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 8, 2013

    POLYURETHANE CONTRAST INJECTION LINE

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DXJ·January 14, 2011

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 8, 2014