BEUDAMED
    16 results · 22ms · Sources: EU EUDAMED, US FDA

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    AlphaVent Knotless SP PEEK Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD ULTRA-FINE¿ MINI PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·May 2, 2019

    BD ULTRA-FINE¿ MINI PEN NEEDLES 5MM (3/16¿) 31G

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·May 7, 2019

    BD INSULIN SYRINGE WITH THE BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·May 12, 2020

    STERISPINE LC CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECTRUM MODULAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD INSULIN SYRINGE WITH BD ULTRA-FINE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 27, 2018

    BD ULTRA FINE¿ PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·April 26, 2019

    BD ULTRA-FINE¿ MINI PEN NEEDLES 5MM (3/16¿) 31G

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·April 11, 2019

    IMPLANT, ENDOSSEOUS, ROOT-FORM

    FDA Adverse Event
    Injury ·J DENTAL CARE SRL·Product code DZE·August 28, 2025

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 6, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 5, 2011

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 18, 2013

    NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·September 2, 2022

    NOVATION CONSTRAINING RING, GROUP 1

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWZ·September 2, 2022

    ACCOLADE DR SL MRI (Model L311)

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