BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Oscillometric Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MECTALIF

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SURGIAID

    FDA 510(k)
    FDA Unclassified ·Unknown

    11G MAMMOMARK BREAST MARKER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code FZP·October 9, 2008

    6000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 14, 2013

    KINETRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·July 29, 2011

    SKINTACT

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code DRX·December 11, 2019

    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 11 X 135 MM, Silicone, Sterile, Item 431191.

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