BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Pioneer Plus Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ECHO HIP SYSTEM INSTRUMENTATION

    FDA UDI
    Biomet Orthopedics, LLC·00880304520660·

    SMOOTH STEINMANN PINS, TROCAR POINT

    FDA UDI
    Biomet Orthopedics, LLC·00887868016660·

    REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    K-SPRAY, MODEL 085-2715

    FDA 510(k)
    FDA Class 1 ·Dental

    IOLMASTER 500

    FDA Adverse Event
    Malfunction ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·October 14, 2015

    FLEXCATH STEERABLE SHEATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC CRYOCATH LP·Product code DRA·July 14, 2011

    X-MESH INSERTER/EXPANDER

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES SPINE·Product code LXH·June 11, 2013

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·September 9, 2008