BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    NMI PORT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ArgenZ HT+ 95x20 D4

    FDA UDI
    ARGEN CORPORATION, THE·D818122767·Dental porcelain/ceramic restoration kit

    HEX-FIX

    FDA UDI
    Smith & Nephew, Inc.·03596010069863·STAINLESS STEEL HALF PIN 6MM X 50MM

    RAICHEM LIPID CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CARDIO XP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VAXCEL WTIH PASV MINI PORT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LJT·October 29, 2007

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·May 21, 2013

    CLINITEK STATUS+

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code JIL·September 26, 2014

    ASR ACETABULAR IMPLANT 50

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·June 3, 2011