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

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    RayStation

    FDA 510(k)
    FDA Class 2 ·Radiology

    10PW - Head Start - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588100937·10PW - Head Start - Poly White

    Medallion®

    FDA UDI
    Merit Medical Systems, Inc.·00884450029978·

    PRESEP OLIGON OXIMETRY CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VSI TORQUE DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·August 14, 2020

    LOGIC CR TIB INSERT SLOPE++, SZ 1, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·November 1, 2022

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·October 10, 2014

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code NPT·June 10, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·July 19, 2019

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 14, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 30, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 28, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 26, 2018

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·September 17, 2019