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

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    Voluson S8/ Voluson S10/ Voluson S10 Expert

    FDA 510(k)
    FDA Class 2 ·Radiology

    FUKUSHIMA SUCTION TUBE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896009677·FUKUSHIMA SUCTION TUBE

    FUKUSHIMA SUCTION TUBE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B0991803740·FUKUSHIMA SUCTION TUBE

    Tibial Alignment Rod

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215063696·

    MAX PULSE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIOSYAG MEDICAL SYSTEM

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

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·October 17, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 20, 2013

    MITEK FMS UNKNOWN TUBING

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code HRX·July 27, 2011

    GALAXY G3 MINI 2MM X 4CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021

    GALAXY G3 5MM X 15CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021

    GALAXY G3 MINI 3MM X 8CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021

    GALAXY G3 MINI 2MM X 3CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021