BEUDAMED
    10 results · 31ms · Sources: EU EUDAMED, US FDA

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    GUIDE WIRE

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

    Ultraverse® 018

    FDA UDI
    Bard Peripheral Vascular, Inc.·00801741054266·Ultraverse® 018 PTA Balloon Dilatation Catheter...

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M3848130260·BioMesh® 3MC - 90 x 92 mm

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M384813026US0·BioMesh® 3MC - 90 x 92 mm

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M384813026CP0·BioMesh® 3MC - 90 x 92 mm

    POWDERED LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Wright Jones Fracture System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·May 15, 2014

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    REPAIR CORE SABER DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·August 12, 2010