BEUDAMED
    66 results · 31ms · Sources: EU EUDAMED, US FDA

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    Currie Medical ALP Pediatric Calf Compression Sleeves (all sizes)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526550223·GENUMEDI PT KNEE SUP SILVER R EW VII

    RESUSCITATION UNIT 105

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OMNILUX PLUS

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 22, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 18, 2015

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 6, 2025

    PENUMBRA SYSTEM JETD REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·May 8, 2019

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 17, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 30, 2015

    PENUMBRA SYSTEM 3MAX REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·June 14, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 26, 2015

    IDENTITY XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC. CRMD·Product code DXY·January 13, 2014

    OBTAPE TRANSOBTURATOR SLING

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE LLC·Product code OTN·May 23, 2013

    TROPONIN T

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MMI·June 29, 2011

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 9, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·September 9, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·September 16, 2015

    PENUMBRA SYSTEM 4MAX REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 30, 2015

    PENUMBRA SYSTEM JETD REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·November 11, 2021