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

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    THE HILL ADJUSTABLE HA90

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MEGA PURE CART

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

    5.0MM TI LOCKING SCR SLF-TPNG W/T25 STARDRIVE 40MM-STERILE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KTT·April 16, 2019

    FRESENIUS 2008K

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 24, 2014

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·January 28, 2013

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 10, 2010

    U-SDN 2 Part Ultra Modified Seldinger Needles, NS/37-0387. All needles were sold in bulk, non-sterile, and intended for further processing. Needles are packaged in zipper-bags, 300 pieces per bag, with shipment occurring in a corrugated cardboard box. Needles consist of a stainless steel cannula with a molded plastic hub. This needle is intended to be placed over the guidewire to enlarge the opening in the vessel. Vessel dilator, for percutaneous catheterization.

    FDA Recall
    Terminated ·Procedure Products, Inc.·Product code DRE·October 27, 2015