BEUDAMED
    14 results · 36ms · Sources: EU EUDAMED, US FDA

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    DADE IMMUNOADSORBED FACTOR IX DEFICIENT PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100400·MELLINGER PHACO SPECULUM

    FLOWIRE AND FLOMAP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MICROZYME TSH ENZYME IMMUNOASSAY KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·June 4, 2014

    HCG COMBO DEVICE SP BRAND RAPID TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·January 9, 2013

    REPLY

    FDA Adverse Event
    Malfunction ·SORIN BIOMEDICA C.R.M., S.R.L.·Product code NVZ·November 4, 2010

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 14, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 3, 2024

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·January 24, 2023

    RADIFOCUS ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·September 26, 2018