BEUDAMED
    235 results · 20ms · Sources: EU EUDAMED, US FDA

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    ACHTUNG TD-4207, CLEVER CHEK TD-4209, CLEVER CHEK TD-4222

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0120050·Screw Sizing Block

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981182502·Trial, 20x15x5mm, 7 deg. Lordosis, w/o Stops

    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

    MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BOLUSPRO ULTRA

    FDA 510(k)
    FDA Class 2 ·Radiology

    GENETIC SYSTEMS HIV-1/HIV-2 PEPTIDE EIA

    FDA Adverse Event
    Other ·BIO-RAD LABORATORIES, INC.·Product code MZF·May 23, 2005

    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

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·February 3, 2006

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·*·Product code GDW·June 2, 2005

    9616026-2006-00240

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