BEUDAMED
    406 results · 23ms · Sources: EU EUDAMED, US FDA

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    iTind System

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

    Trinity Acetabular Hip System

    FDA UDI
    CORIN LTD·05055343895986·TRINITY SPRUNG INTRODUCER HANDLE

    SOFTSILK

    FDA UDI
    Smith & Nephew, Inc.·03596010510761·9 X 25 MM SOFTSILK 1.5 SCREW ...

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319706435·Lahey Skin Hook 4-3/4" (11.9cm), 2 sharp prongs

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C31422101380·Titanium PLIF Spacer, 22 x 10 x 13mm, 8 deg

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C30422101380·PEEK PLIF Spacer, 22 x 10 x 13mm, 8 deg

    PAIRED HYDROGEL ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    PROFILE II ER

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    BD DISCARDIT II 2-PIECE SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·January 28, 2023

    HARMONIC ACE 23 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code LFL·October 20, 2008

    UNICEL DXH 800 COULTER CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·August 5, 2011

    ACUITY

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code OJX·July 8, 2013

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 14, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026