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

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    illumigene Mycoplasma DNA Amplification Assay

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·24026704509014·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100691·MAUMENEE-PARK SPECULUM SOLID

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702898699·ELVAREX FORTE 3/KNEE HIGH/SLANT-OPEN TOE-ELEPHA...

    BAK®

    FDA UDI
    ZIMMER SPINE, INC.·00889024333284·

    II Ring Retractor

    FDA UDI
    Automated Medical Products Corp.·00810118341489·Malleable Retractor 6" x 9" with Protective Edge

    PROVISIONAL INLAY/ONLAY KIT

    FDA 510(k)
    FDA Class 2 ·Dental

    SUNTOUCH TOPICAL HEMOSTATIC DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 12, 2024

    COLLEAGUE PRE-P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code LWP·June 8, 2013

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·October 8, 2014

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026

    METACROSS OTW PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2019

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

    OHICHO NEO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 7, 2024