BEUDAMED
    11 results · 23ms · Sources: EU EUDAMED, US FDA

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    BED PATIENT MONITOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209136063·

    EMIT AMITRIPTYLINE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    VISION POTASSIUM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 9, 2014

    ATTAIN OTW

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 5, 2010

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 20, 2012

    BMET ARCOM AP PAT W/WIRE 31MM IRE 31MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·May 5, 2022

    BIOMET ILOK PRI TIB TRAY 63MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 5, 2022

    VNGD CR TIB BRG 10X63/67 MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 5, 2022

    VANGUARD CR INTERLOK FEM - RT 60

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 5, 2022