BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    Fiber Laser Treatment System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074362489·SCREW 7221770 HA COATED CANN 7.5 X 70

    SIGVARIS, INC.

    FDA registration
    SIGVARIS, INC.·8 products·🇺🇸 United States

    Masimo Rad-G Pulse Oximeter, Masimo Rad-G YI sensor, Masimo Rad-G Reusable sensor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEADSTAR MEDICAL SMALL VOLUME JET NEBULIZER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RAD-G

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code DQA·October 17, 2024

    OXF ANAT BRG RT MD SIZE 5 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·August 16, 2022

    OXF UNI TIB TRAY SZ D RM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·August 16, 2022

    66OD X 60 ID MAGNUM ABX PF CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 3, 2018

    M2A-MAGNUM MOD HD SZ 60MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 3, 2018

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·August 17, 2011

    OMNIFIT SER. II CUP INS. 0 DEG.

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·November 3, 2014

    ENDOGIA UNIVERSAL STAPLER - AUTOSUTURE STAPLERS

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GDW·July 6, 2013