BEUDAMED
    11 results · 36ms · 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.

    BAXA PCA INFUSOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756349567·EXTREMITY PACK

    DIAMOND-FLEX(R) GRASPERS

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

    ZOLL M SERIES

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    CUP: MPACT ACETABULAR SHELL DIAMETER 52 TWO-HOLES

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·July 28, 2021

    ATTUNE PS RP INSRT SZ 5 14MM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code NJL·December 31, 2025

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·November 22, 2010

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 2, 2014

    GOBED II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·December 19, 2012

    BD FACSLYRIC¿ 3L12C INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code OYE·October 17, 2022

    BD FACSLYRIC¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code OYE·February 27, 2023