BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    ProRad 2FC and ProRad 3NC Stationary Radiographic Systems

    FDA 510(k)
    FDA Class 2 ·Radiology

    Vanguard Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304673823·

    Vanguard Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304647909·

    Crosslink, Small, with T-15 Driver

    FDA UDI
    XENCO MEDICAL LLC·B064XM21835411·

    I-STAT EC8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CHL·March 20, 2019

    BD INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·March 27, 2025

    NEONATE HEAD AND BODY COILS

    FDA 510(k)
    FDA Class 2 ·Radiology

    CLEARSTART SVM SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    2183541-1997-00060

    FDA Adverse Event
    Injury ·Product code ESW·June 13, 1997

    2183541-1997-00011

    FDA Adverse Event
    Injury ·Product code MAF·March 11, 1997

    VANGUARD CR ILOK FEM-RT 67.5

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    VG CR RET LIP TIB BRG 11X71/75

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 18, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

    INTROCAN SAFETY

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL·Product code FOZ·July 27, 2011