BEUDAMED
    12 results · 33ms · Sources: EU EUDAMED, US FDA

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    syngo. CT Single Source Dual Energy (twin beam)

    FDA 510(k)
    FDA Class 2 ·Radiology

    VERSANT VALUE

    FDA UDI
    FGX INTERNATIONAL INC.·00193033307755·

    ORION MICRO CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    2MP MEDICAL MONOCHROME REFERENCE DISPLAY, MODEL MDM2130-2NC

    FDA 510(k)
    FDA Class 2 ·Radiology

    BALL HEADS: MECTACER HEAD BIOLOX OPTION Ø 28

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·August 20, 2024

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013

    ARTICUL/EZE M HEAD 36MM +8.5

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·July 8, 2011

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 9, 2008

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQO·January 18, 2019

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·November 26, 2019

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·November 26, 2025

    CUP: MPACT ACETABULAR SHELL Ø50 TWO-HOLES

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·January 26, 2022