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

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    VALTRAC (BAR) REMOVER DEVICE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108383·ANIS NEEDLE HOLDER CURVED WITH LOCK

    EXTRACORPOREAL SUBCLAVIAN CATHETER KIT

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

    LIFESENSE, MODEL LS1-9R

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·October 11, 2010

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 1, 2012

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·June 10, 2014

    Connecting Tube - Female to Male Luer Lock, HPCT8.8-30-M-FM Product Usage: The connecting tube is intended to be a conduit between a fluid reservoir and a vascular catheter in the patient. The connecting tube may be used during angiographic procedures to connect radiographic contrast power injector to a vascular catheter, arterial pressure monitoring, and fluid infusion.

    FDA Enforcement
    Class II ·Terminated·Cook Inc.·May 16, 2018