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

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    PEREGRINE 23GA CURVED LASER PROBE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LIFEJET F16 HEMODIALYSIS/APHERESIS CHRONIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    GUIDED MEDICAL POSITIONING SYSTEM II (GMPS II)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CORDLESS DRIVER 3

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HRX·May 21, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011

    Depuy P.F.C. E knee system, TC3 tibial insert; polyethylene tibial insert, Sz 4, 17.5 mm; Ref 96-0543.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005