BEUDAMED
    28 results · 24ms · Sources: EU EUDAMED, US FDA

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    DC-7 DIAGNOSTIC ULTRASOUND SYSTEM, DC-3/DC-3T DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814565·GENUMEDI SAND SIZE V

    ACCUPROBE

    FDA UDI
    Hologic, Inc.·15420045506176·

    ProCide-D

    FDA UDI
    METREX RESEARCH, LLC·00615375005507·Sterilizing & Disinfecting Solution 28Day Glut...

    LIQUICHEK BLOOD GAS PLUS E CONTROL, MODEL 576, 577, 578

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SUPERSTITCH VASCULAR SUTURING DEVICE

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

    BIPAP A30

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 31, 2022

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AVAPS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 3, 2022

    BIPAP A30

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AVAPS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP A30

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 30, 2022

    BIPAP AVAPS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 16, 2022

    BIPAP AVAPS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP ST

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    IN TOUCH EU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 9, 2013

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - GUANGZHOU·Product code KDI·September 19, 2014