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

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    TEFLON-COATED HYPODERMIC NEEDLES/REGIONAL BLOCK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704290295·

    ACS HI-TORQUE TAPERED DIAMETER GUIDE WIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TECHNICON H.1 SYSTEM, T LYMPHOCYTES METHOD

    FDA 510(k)
    FDA Class 2 ·Hematology

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 10, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·December 10, 2012

    DA VINCI BALLOON PORT

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code NAY·September 28, 2010

    PLATE GC LECT AGAR 90MM 20

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JTY·March 29, 2021

    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 15 X 200 MM, Silicone, Sterile, Item 431198.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020