BEUDAMED
    134 results · 21ms · Sources: EU EUDAMED, US FDA

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    BUZZAROUND, VEHICLE, MOTORIZED 3-WHEELED

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Septal splints

    FDA UDI
    Spiggle & Theis Medizintechnik GmbH·04250381809785·FEP, standard 0.25 m...

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00810094578312·One Scope Pro -Adult Angulated Size 4 Blade

    Septal splints

    FDA UDI
    Spiggle & Theis Medizintechnik GmbH·04250381809792·FEP, standard 0.25 m...

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 10, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

    FORTAFLEX SURGICAL MESH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LIFECARD CF COMPACT RECORDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 4, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·July 8, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK USA, INC.·Product code KWP·October 30, 2019

    9616026-2006-00240

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616026-2006-00244

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 9, 2019