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

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    ATRIUMS PDR THORACIC CATHETER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909126452·REVELATION DIAMOND 850L-016C - 5 PACK

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110904·TIP GUARDS VENTED ORANGE PACK OF 100

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110881·TIP GUARDS VENTED RED PACK OF 100

    REPROCESSED EBI EXTERNAL FIXATION DEVICES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RADIFORCE LARGE MONITOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GEMSTR 7 THPY ALT ST

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 14, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 14, 2013

    FREESTYLE AORTIC ROOT BIOPROSTHESIS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES, INC.·Product code LWR·November 24, 2010