BEUDAMED
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    Q BIO

    FDA registration
    Q BIO·2 products·🇺🇸 United States

    Constellation

    FDA UDI
    Q Bio, Inc.·00860011384809·Constellation is an automated image post-proces...

    CHOLESTEROL BIO METER BY Q.STEPS

    FDA Adverse Event
    Malfunction ·BIOMEDIX, INC. USA·Product code CGA·September 24, 2014

    SMITH & NEPHEW BIORCI DRIVER

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC./ENDOSCOPY DIVISION·Product code HXX·November 2, 2000

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·April 27, 2023

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·April 27, 2023

    SAPPHIRE INFUSION PUMP

    FDA Adverse Event
    Malfunction ·Q CORE MEDICAL LTD·Product code FRN·November 20, 2018

    FISHER & PAYKEL 850 RESPIRATORY HUMIDIFICATION SYSTEM

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTH CARE INC.·Product code BTT·December 20, 2001

    POWER SUPPLY

    FDA Adverse Event
    Malfunction ·Q CORE MEDICAL LTD.·Product code MRZ·December 10, 2015

    BIOTRUE

    FDA Adverse Event
    Injury ·Product code LYL·May 27, 2014

    ARTIS Q ZEEGO

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH-AT·Product code OWB·February 15, 2023

    2.8MM Q-FIX ALL SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code MBI·October 23, 2025

    QFIX 1.8 MINI SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code MBI·October 27, 2025

    2.8MM Q-FIX ALL SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code MBI·October 23, 2025

    ADVIA CENTAUR CP TROPONIN ULTRA (TNI-ULTRA) ASSAY

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·August 23, 2016

    DISPOSABLE KIT FOR 1.8MM SHOULDER Q-FIX

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code LXH·January 15, 2021

    #1 ESCORT VISION CENTRAL STATION

    FDA Adverse Event
    Death ·MEDICAL DATA ELECTRONICS (INVIVO MDE)·Product code DRG·December 29, 2004

    2.8MM Q-FIX ALL SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code MBI·January 24, 2025

    1.8MM Q-FIX ALL SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code MBI·January 22, 2025

    BIOCOMPOSITE INTERFERENCE SCREW W/ DISP. SHEATH

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MAI·July 1, 2015