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

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    MOSAIQ Oncology Information System

    FDA 510(k)
    FDA Class 2 ·Radiology

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304270558·

    Percutaneous Compression Plate (PC.C.P)

    FDA UDI
    ORTHOFIX SRL·18032568866261·GOTFRIED PC.C.P. SHAFT SCREW 34MM

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528128268·3.0 X 34mm Cannulated Headed Screw, T10

    Percutaneous Compression Plate (PC.C.P)

    FDA UDI
    ORTHOFIX SRL·18033509850608·GOTFRIED PC.C.P. SHAFT SCREW 34MM STERILE

    FOTONA XD-2 DIODE LASER SYSTEM, MODEL MD01-2F

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

    GENESYS SPINE INTERBODY FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

    BIOMET ARCOM ALL POLY PAT BUTTON

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·February 24, 2017

    VANGUARD CR-LIPPED TIBIAL BEARING 10MM X 79/83MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·February 24, 2017

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·October 17, 2014

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS-FREIBURG·Product code JEY·June 21, 2013

    URETERAL INDWELLING CATHETER/STENT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FAD·July 28, 2011

    VANGUARD CR ILOK FEM-LT 75

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRY·December 13, 2018