BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    URINARY DRAINAGE BAG

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

    UNISYN IMAGE FUSION, VERSION 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    MICROPULSE 26U PULSE GENERATOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    BICART

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KPO·April 30, 2014

    INFUSO.R.

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 11, 2012

    LIGACLIP MCA SMALL APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC (CINCINNATI)·Product code GDO·January 30, 2008

    Haemonetics cardioPAT -Cardiovascular Perioperative Autotransfusion System Model 2050 US Models Out-Side the US: 02050-UK, 02050-ES, 02050-IT, 02050-NL, 02050-GE, 02050-FR, 02050-JA The Haemonetics Cardiovascular Perioperative Autotransfusion System for Use (cardioPAT) is indicated for use to salvage red blood cells from blood lost intraoperatively and postoperatively during cardiovascular surgical procedures, where the expected rate of processing of salvaged blood and fluid aspirated from the surgical site is less than or equal to two liters per hour.

    FDA Recall
    Terminated ·Haemonetics Corporation·Product code CAC·July 27, 2011