BEUDAMED
    10,000 results · 42ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    microFibre® Electrode

    FDA UDI
    ELLIQUENCE, LLC·00846338000035·

    Carriere

    FDA UDI
    Ortho Organizers, Inc.·00190707046132·.019 x .025 M-Series Stainless Steel D-LX, Sing...

    Plasdent

    FDA UDI
    PLASDENT CORPORATION·D832MFA1·Model Formers Kit - 6 Pieces Assorted Sizes

    CARELINK PERSONAL MMT-7333

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·August 31, 2023

    BD PYXIS¿ ES SERVER

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·November 24, 2025

    SMARTPHONE ANDROID APP: PUMP CONNECT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code PKU·March 31, 2023

    CARELINK CONNECT APP IOS

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code PKU·September 1, 2023

    CARELINK CONNECT APP ANDROID

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code PKU·September 11, 2023

    VBEAM PRIMA LASER SYSTEM

    FDA Adverse Event
    Injury ·CANDELA CORPORATION·Product code GEX·August 11, 2025

    9MM TI CANNULATED TIBIAL NAIL-EX/270MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code JDS·May 11, 2015

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·August 2, 2019

    PROMUS PREMIER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·February 10, 2021

    MUSTANG?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·May 12, 2014

    VBEAM PRIMA LASER SYSTEM

    FDA Adverse Event
    Injury ·CANDELA CORPORATION·Product code GEX·August 11, 2025

    SMARTPHONE IOS APP: PUMP CONNECT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code PKU·May 21, 2025

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·December 23, 2019

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·June 21, 2018

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·June 21, 2018

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH HI-TEC, INC.·Product code KHO·March 24, 2022

    1-DAY ACUVUE MOIST FOR ASTIGMATISM

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON VISION CARE, INC. ¿ US·Product code LPL·October 13, 2015