BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    Intermittent nelaton catheter for single use

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

    TRIAL HEAD FOR BROACH ESOP HA D.32 -3,5

    FDA UDI
    FOURNITURES HOSPITALIERES INDUSTRIE·03661489226779·

    MEDLEY SPO2 MODULE, MODEL 8210 & SPO2 SENSORS & CABLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    aboNT SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·October 31, 2014

    FLEXCATH STEERABLE SHEATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC CRYOCATH LP·Product code DRA·August 25, 2011

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 12, 2013

    SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini Implantable Fusion Stimulators are indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels

    FDA Enforcement
    Class I ·Terminated·Zimmer Biomet, Inc.·November 7, 2018