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

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    Powder Free Vinyl Patient Examination Gloves, Clear (non-colored)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LeMaitre Aortic Occlusion Catheter

    FDA UDI
    Lemaitre Vascular, Inc.·00840663101641·LeMaitre Aortic Occlusion Catheter, 8F, eIFU

    LeMaitre Aortic Occlusion Catheter

    FDA UDI
    Lemaitre Vascular, Inc.·00840663101634·LeMaitre Aortic Occlusion Catheter, 8F

    VEO® Lateral Interbody Fusion System

    FDA UDI
    Choice Spine, LP·00840996134002·LATERAL,ANGLED TRIAL,0DEG,17X13

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319722404·Millard Double Hook Forceps 6" (15cm), with thu...

    ELITECH CLINICAL SYSTEMS BILIRUBIN TOTAL 4+1, ELITECH CLINICAL SYSTEMS ELICAL 2, ELITECH CLINICAL SYSTMES ELITROL I & II

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TROCHANTERIC NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    I-STAT 6+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·September 28, 2021

    UNKNOWN URETEX MESH PRODUCT

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·October 29, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 12, 2011

    FORTIFY DR, DF4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 8, 2013

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 18, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·October 23, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 20, 2021

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 18, 2021

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 20, 2021

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 18, 2021

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·February 25, 2021