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

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    ENDOWASH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Damon 3

    FDA UDI
    ORMCO CORPORATION·00889989052794·L4R DAMON 3 .022 -12/+2/0 HK

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100448·LESTER-BURCH EYE SPECULUM

    CARDIOCAP DR-124 RECORDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFIED SITE PERISTALTIC FOOTSWITCH

    FDA 510(k)
    FDA Class 1 ·Dental

    FR3, REFURB ECG AED - US ENGLISH

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 12, 2014

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·January 10, 2013

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 25, 2008