BEUDAMED
    10,000 results · 104ms · 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 ×

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·April 4, 2012

    STEM: AMISTEM-P COLLARED AMISTEM-P COLLARED STD STEM SIZE 3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·February 8, 2023

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 15, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 15, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 5, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 15, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 5, 2024

    EVOKE CAP12 PERCUTANEOUS LEAD KIT - 60CM (US)

    FDA Adverse Event
    Injury ·SALUDA MEDICAL PTY LTD·Product code LGW·July 2, 2025

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 5, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 15, 2024

    HYLAFORM PLUS

    FDA Adverse Event
    Injury ·GENZYME BIOSURGERY·Product code LMH·March 28, 2005

    ROTAFLOW CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·February 22, 2016

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS LLC·Product code OYC·March 2, 2019

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS LLC·Product code OYC·February 6, 2019

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS LLC·Product code OYC·February 28, 2019

    UNKNOWN

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·March 16, 2026

    REMUNITY PUMP FOR REMODULIN (TREPROSTINIL) INJECTION

    FDA Adverse Event
    Malfunction ·MILLYARD ADVANCED MEDICAL PRODUCTS, LLC·Product code QJY·March 30, 2026

    DX FIBERTAK SUTURE ANCHOR, #2 MTS W/ NDL

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·February 24, 2026

    DX FIBERTAK SUTURE ANCHOR, #2 MTS W/ NDL

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·February 24, 2026

    BIO-COMP SWVLK C, CLD 4.75X19.1MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MAI·March 3, 2026