BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Infrared Thermometer, model: PC808

    FDA 510(k)
    FDA Class 2 ·General Hospital

    T

    FDA Adverse Event
    Malfunction ·CONCORD MANUFACTURING·Product code KDI·November 20, 2017

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930719071710·Box Curette 7x17 ang.

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930719071700·Box Curette 7x17 str.

    FLEX-TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    KONICA MINOLTA XPRESS DIGITAL MAMMOGRAPHY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SKINTACT

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code MKJ·November 21, 2019

    N/A

    FDA Adverse Event
    Malfunction ·ASCENT HEALTHCARE SOLUTIONS·Product code NLQ·October 6, 2008

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code LPH·June 26, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·July 29, 2011