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

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    Amendia Interbody Fusion Devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Scorpio

    FDA UDI
    Howmedica Osteonics Corp.·07613154020690·Cruciate Retaining Tibial Insert

    DISPOSABLE SPETZLER-MALIS DUAL IRRIGATING BIPOLAR FORCEPS

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

    JSZ MULTIACTION GP CONTACT LENS SOLUTION

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    OXIMAX N-595 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code DQA·June 16, 2011

    COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 17, 2008

    NEEDLE 27GA 1/2IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·June 2, 2020

    Heritage Labs Appraise A1c Diabetes Home Test , Product K7609, 24 kits/shipping carton (Product K7609), each kit packed in a box and contains 1 Triad Medium Alcohol Prep Pad, Cat. No. 10-3001, NDC 50730-3001-0, and blood specimen collection supplies, forms, and instructions Blood specimen collection

    FDA Recall
    Terminated ·Heritage Labs International LLC·Product code LCP·January 9, 2011