BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Akros Fibulink Syndesmosis Repair Kit

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814565·GENUMEDI SAND SIZE V

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111402050·LISTER TC BANDAGE SCISSORS5.5 INCHES

    KIMGUARD ONE-STEP STERILIZATION WRAP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODIFICATION TO ENDO-EASE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CROSSFIRE 0 DEG INSERT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 22, 2019

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011

    GYNECARE PROLIFT TOTAL PELVIC FLOOR REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·June 11, 2013

    TWINFIX TI 5.0 ANCHOR W/DURABRAID

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Product code MBI·September 8, 2008