BEUDAMED
    16 results · 23ms · Sources: EU EUDAMED, US FDA

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    LIQUICKEK IMMUNOASSAY PLUS CONTROL, LEVEL 1 MODEL 267, LIQUICHEK IMMUNOASSAY PLUS CONTROL, LEVEL 2 MODEL 268, LIQUICHEK

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ArgenZ HT+ 98x25 A1

    FDA UDI
    ARGEN CORPORATION, THE·D818122838·Dental porcelain/ceramic restoration kit

    N/A

    FDA UDI
    SALTER LABS·00607411889882·Nasal Cannula (adult) Salter Style® with 50’ (1...

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·March 31, 2016

    FOTONA DUALIS ER:YAG/KTP LASER SYSTEM

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

    PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TARGET DEVICE 300X160MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·March 2, 2012

    PROWLER SELECT MICROCATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code KRA·May 21, 2013

    FREESTYLE FREEDOM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 14, 2008

    UNKNOWN DEPUY ASR HIP

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

    TALENT TAA STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·November 30, 2016

    VALIANT STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·November 29, 2016

    ENDURANT-II

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·November 30, 2016

    VALIANT STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·November 29, 2016

    ENDURANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·November 30, 2016

    VALIANT STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·November 30, 2016