BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Maxima XTEND Handpiece Maintenance System

    FDA 510(k)
    FDA Class 1 ·Dental

    EPI-K

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    TRILLIANT SURGICAL SUBTALAR IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD INSYTE AUTOG BC

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 1, 2024

    IN TOUCH EU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 3, 2013

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 28, 2011

    VANGUARD CR FEMORAL

    FDA Adverse Event
    Injury ·BIOMET INC.·Product code JWH·September 3, 2008

    Azurion 3 M12; Catalog numbers: (1) 722063, (2) 722221.

    FDA Enforcement
    Class I ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025