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

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    LUMILOC (TM) SAFETY INTRODUCER NEEDLE

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

    IVD (IN VIVO DOSIMETER), MODEL 1131

    FDA 510(k)
    FDA Class 2 ·Radiology

    SCREENERS BENZODIAZEPINE (BZD) TEST, DRUG SCREEN DIP BENZODIAZEPINE (BZD) TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    NV GXL LINR, NTRL, 32MM ID, GROUP 2 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code MEH·July 20, 2022

    NV GXL LNR, LIPPED, 36MM ID, GROUP 3 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·July 9, 2024

    DEXTRUS 4137

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·April 22, 2013

    GOBED II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·March 29, 2011

    ACUSNARE POLYPECTOMY SNARE SUPPLIED IN BOXES OF 10

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code FDI·July 3, 2008

    NV GXL LINR, NTRL, 28MM ID, GROUP 1 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 11, 2024

    NV GXL LINR, NTRL, 36MM ID, GROUP 3 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 28, 2024