BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    COROMETRICS 120 SERIES MATERNAL/FETAL MONITOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SUCTION TUBE

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

    BURTON HAND HELD SLIT LAMP - MODEL SL750

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MODULAR TAPERLOC FEMORAL POROUS COATED 7.5 X 135MM TYPE I TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·July 25, 2017

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 29, 2014

    BIOMET StageOne Knee Tibial Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 433165.

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