BEUDAMED
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    BONE WIRE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5820306650·SCISSORS, SURGICAL TISSUE, DENTAL

    Atmos

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746150968·SUPPLIES ATMOS THERMOFORMING MATERIAL .035 120m...

    ERIKA DE REYNOSA, S.A. DE C.V.

    FDA registration
    ERIKA DE REYNOSA, S.A. DE C.V.·10 products·🇲🇽 Mexico

    FADASSI MEDICAL FM-1 NO BLENDER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TFX MEDICAL SAFETY NEEDLE WITH INTRODUCER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PRIMING SET FOR ARTERIAL BLOODLINES

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code KOC·January 9, 2014

    PRIMING SET FOR ARTERIAL BLOODLINES

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code KOC·January 9, 2014

    PRIMING SET FOR ARTERIAL BLOODLINES

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code KOC·January 9, 2014

    PRIMING SET FOR ARTERIAL BLOODLINES

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code KOC·January 9, 2014

    PRIMING SET FOR ARTERIAL BLOODLINES

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code KOC·January 9, 2014

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code FKX·January 24, 2014

    LIBERTY CYCLER SET, DUAL PATIENT CONNECT

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code FKX·August 14, 2013

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code FKX·April 30, 2013

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code FKX·April 30, 2013

    8030665-2003-00118

    FDA Adverse Event
    Malfunction ·REYNOSA MFG·Product code FJK·September 24, 2003

    8030665-2000-00247

    FDA Adverse Event
    Injury ·Product code FJK·August 18, 2000

    8030665-2007-00015

    FDA Adverse Event
    Death ·REYNOSA MANUFACTURING·Product code FJK·March 15, 2007

    8030665-2005-00092

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code FKX·December 20, 2005

    8030665-2006-00254

    FDA Adverse Event
    November 30, 2006