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

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    Filters Regulation: Us FDA ×

    GripMate

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Universal Digital Interface 2W, UDI 2W

    FDA 510(k)
    FDA Class 2 ·Radiology

    UCR SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·August 9, 2021

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 23, 2024

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·November 7, 2008

    SENSOR MMT-7002C,10PK, GLUCOSE, BSA,17L

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·September 1, 2011

    LIBERTY CYCLER

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FKX·July 19, 2013

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·October 16, 2017

    TECNIS SIMPLICITY

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·February 7, 2023