BEUDAMED
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    URETERAL ILLUMINATOR

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

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150737·K-WIRE - SINGLE TROCAR 1.0mm DIA x 150mm

    MICROSPAN SYSTEM

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code FED·June 8, 2006

    INTRAVASCULAR ACCESS INTRODUCER SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MCC Para-Fix CARY BLAIR MEDIUM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    INTERLINK CONTINU-FLO, 3 INJECTION SITES, LUER LOCK, 105"

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SHERBROOKE·Product code FPA·December 29, 2010

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·February 4, 2013

    AGC KNEE IMPLANT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·July 17, 2014