BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Cocoon Portable Handheld X-Ray System

    FDA 510(k)
    FDA Class 2 ·Dental

    Endo Paddle Retract

    FDA UDI
    Covidien LP·10884523000771·Paddle Retractor

    HOSMAN USB BLOOD PRESSURE MONITOR; WRIST TYPE AND UPPER ARM TYPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ETHICON ENDO SURGERY ARTICULATING NEEDLE KNIFE, MODEL 2504

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ENDO PADDLE RETRACT

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GAD·February 29, 2024

    ENDO PADDLE RETRACT

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GAD·January 7, 2025

    ENDO PADDLE RETRACT

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GAD·January 7, 2025

    ENDO PADDLE RETRACT

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GAD·February 12, 2025

    ENDO PADDLE RETRACT

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GAD·February 12, 2025

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 30, 2013

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 23, 2011

    BRAVO

    FDA Adverse Event
    Malfunction ·ARIZONA DEVICE MANUFACTURING·Product code FFT·September 19, 2008

    ENDO PADDLE RETRACT

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GAD·December 2, 2022

    ENDO PADDLE RETRACT

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GAD·December 2, 2022