BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON

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

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009

    IONTOPHORESIS DEVICE, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VAC - RITE RIGHT ANGLE ASPIRATOR TUBE & HOLDER

    FDA 510(k)
    FDA Class 1 ·Dental

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMELRY NELLCOR·Product code CBK·May 30, 2014

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·February 15, 2013

    REFURBED COLLEAGUE CX TRIPLE CCHANNEL VOLUMETRIC INFUSION PU

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 20, 2011

    InterGard Knitted Collagen Coated Vascular prostheses marketed under 510(k) # K964625; InterGard Woven Collagen Coated Vascular prostheses marketed under 510(k} #K970843 and K984294.

    FDA Recall
    Terminated ·Intervascular S.A.S. Zone Industrielle Athelia I La Ciotat Cedex France·Product code DSY·December 9, 2009