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

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    CROSS-CHECKS P

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Medline

    FDA UDI
    MEDLINE INDUSTRIES, INC.·10888277940918·MINOR BIOPSY KIT

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111031·INSTRUMENT CADDY LARGE

    Lacrimal Dilator

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108666·CASTROVIEJO LACRIMAL DILATOR

    NEXGEN CR FEMORAL COMPONENT

    FDA Adverse Event
    Death ·ZIMMER, INC.·Product code HSA·November 22, 1996

    SIEMENS

    FDA Adverse Event
    Injury ·SIEMENS·Product code CBK·May 16, 1997

    POWDER FREE NATURAL RUBBER LOW MODULUS LATEX PATIENT EXAMINATION GLOVES WITH A PROTEIN LABELING CLAIM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CoLink View Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FPO·December 30, 2010

    WALLFLEX¿ COLONIC

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code MQR·February 21, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 31, 2014