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

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    SILIMED PECTORAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SlimLine®

    FDA UDI
    ZIMMER SPINE, INC.·00889024404236·

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710410420540·Anterior Closing Wedge Osteotomy Guide, 42mm x ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420420540·Anterio Lateral Closing Wedge Osteotomy Guide, ...

    X-SEPT TRANSSEPTAL SHEATH AND TRANSITION CATHETER, MODEL MV-03-09-90, MV-03-10-90, MV-03-11-90, MV-03-09-120, MV-03-10-1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL SE-312

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AISYS

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·January 18, 2016

    AISYS

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·January 15, 2016

    COLORADO 2 SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWP·January 22, 2009

    COLORADO 2 SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·February 23, 2012

    PREMIUM 6500

    FDA Adverse Event
    MEDTRONIC·Product code LDF·April 5, 2013

    INRATIO

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code GJS·March 25, 2011

    VITALITY DR HE

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 24, 2016