BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

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    BRAIN HEART INFUSION AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    GISH TUBING AND CONNECTORS WITH GBS COATING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REMSTAR SE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·METRO 55 (METHAFILCON A)

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·METRO 55 (METHAFILCON A)

    DORMA 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 16, 2022

    SUPARTZ

    FDA Adverse Event
    Injury ·SEIKAGAKU CORPORATION·Product code MOZ·May 23, 2014

    PFC SIGMARP STB TB IN 3 15.0

    FDA Adverse Event
    Injury ·DEPUY IRELAND·Product code NJL·November 13, 2012

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FNL·September 7, 2010

    ACCOLADE SR SL MRI (Model L310)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025