BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    COBE PATIENT MONITORING PRODUCTS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Mediflex Modular III Basic Laparoscopic Instruments

    FDA UDI
    FLEXBAR MACHINE CORPORATION·00842102103735·Modular 3 DA Wave Grasp Ratcheted Handle/Shaft...

    ISOSEEDS I-125

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODULAP LOOP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 25, 2024

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·June 4, 2018

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code CBK·May 21, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·January 17, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010