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

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    CLEAN-CUFF

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517195463·Brigade Trial, 20x38x32mm 12°

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517401144·Brigade Implant, 20x38x28mm 12°

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150652·K-WIRE - SINGLE TROCAR THREADED 2.0mm DIA x 200mm

    iNSitu™ Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127021732·Cup Manipulator

    3 TO 1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 14, 2011

    3-TO-1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHMAND·Product code DTQ·December 14, 2011

    PERIPHERAL CUTTING BALLOON SMALL MONORAIL OR OVER-THE-WIRE DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MammoGRIP

    FDA 510(k)
    FDA Class 2 ·Radiology

    REVO MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWP·February 9, 2013

    ACTIVA PC

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·January 4, 2011

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Injury ·ZOLL MANUFACTURING CORPORATION·Product code MVK·July 17, 2014