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

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    IMMUNLITE INTACT PTH

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TOMEY PROTON TONOMETER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HUDSON SHERIDAN/HVT TRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·January 23, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 4, 2014

    JAGWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code EZB·December 21, 2010

    SHELL POROUS WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LPH·May 26, 2017

    M2A 38MMX48MM CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 21, 2019

    TAPERLOC POR FMRL LAT 10X140

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MEH·July 23, 2019

    12MM/130 DEG TI CANN TFNA 420MM/LEFT-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HSB·June 2, 2016

    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 9 X 200 MM, Silicone, Sterile, Item 431195.

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