BEUDAMED
    13 results · 21ms · 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 ×

    MEDLINE BLOOD PRESSURE TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707002918·COIL SPRING MEMORIA KIT

    NA

    FDA UDI
    STRYKER CORPORATION·04546540466891·9.5mm x 10.4mm Boring Tool

    NA

    FDA UDI
    STRYKER CORPORATION·04546540466945·9.5mm x 10.4mm Boring Tool

    HERMES OPERATING ROOM CONTROL CENTER

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

    SPRINTER LEGEND 1.25MM RX AND SPRINTER LEGEND 1.25MM OTW BALLOON

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD NANO¿ PRO ULTRA-FINE¿ PEN NEEDLES 32G X 4MM (100 COUNT)

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·April 13, 2023

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 20, 2025

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 22, 2024

    PEN NDL 32G 4MM PRO 100 BOX 1200 CA

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·February 27, 2025

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·May 21, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

    DENALI PEDICLE

    FDA Adverse Event
    Injury ·K2M, INC·Product code KWP·September 5, 2008