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

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    ETEST Meropenem/Vaborbactam (MEV) (0.004/8-64/8 µg/mL)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Percutaneous Compression Plate (PC.C.P)

    FDA UDI
    ORTHOFIX SRL·18032568866254·GOTFRIED PC.C.P. SHAFT SCREW 31MM

    Percutaneous Compression Plate (PC.C.P)

    FDA UDI
    ORTHOFIX SRL·18033509850592·GOTFRIED PC.C.P. SHAFT SCREW 31MM STERILE

    8.3MHZ PENCIL PROBE 7'

    FDA UDI
    PARKS MEDICAL ELECTRONICS, INC.·00816787021011·

    BMR FACE

    FDA 510(k)
    FDA Class 2 ·Neurology

    PORTEX UNIPERC PERCUTANEOUS DILATION TRACHEOSTOMY KIT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CORIN OPTIMIZED POSITIONING SYSTEM

    FDA Adverse Event
    Malfunction ·OPTIMIZED ORTHO PTY LTD·Product code LZO·December 11, 2019

    CORIN OPTIMIZED POSITIONING SYSTEM

    FDA Adverse Event
    Injury ·OPTIMIZED ORTHO PTY LTD·Product code LZO·December 2, 2019

    CORIN OPTIMIZED POSITIONING SYSTEM

    FDA Adverse Event
    Malfunction ·OPTIMIZED ORTHO PTY LTD·Product code LZO·February 12, 2020

    CORIN OPTIMIZED POSITIONING SYSTEM

    FDA Adverse Event
    Malfunction ·OPTIMIZED ORTHO PTY LTD·Product code LZO·December 11, 2019

    CORIN OPTIMIZED POSITIONING SYSTEM

    FDA Adverse Event
    Malfunction ·OPTIMIZED ORTHO PTY LTD·Product code LZO·December 10, 2019

    CORIN OPTIMIZED POSITIONING SYSTEM

    FDA Adverse Event
    Injury ·OPTIMIZED ORTHO PTY LTD·Product code LZO·December 10, 2019

    CORIN OPTIMIZED POSITIONING SYSTEM

    FDA Adverse Event
    Injury ·OPTIMIZED ORTHO PTY LTD·Product code LZO·December 11, 2019

    I-STAT 6+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·May 22, 2019

    GE OEC 9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 3, 2008

    PRECISION®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 21, 2013

    PROXIMATE ILS CURVED CIR STAPL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 28, 2011

    DILATOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DRE·August 13, 2021

    DILATOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DRE·July 27, 2022

    COONS DILATOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DRE·July 28, 2022