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

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    Filters Regulation: Us FDA ×

    DGTX FLEX REAGENT CARTRIDGE, MODEL DF36

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    FUL-VUE ASPHERIC CATARACT LENS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    RecoveryRx

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    INDIGO 1.0CM LASER FIBER

    FDA Adverse Event
    Death ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GEX·June 22, 2006

    RADIFOCUS OPTITORQUE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 5, 2013

    STAN S31 FETAL HEART MONITOR

    FDA Adverse Event
    Death ·NEOVENTA MEDICAL AB·Product code HEO·February 10, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·August 7, 2014

    OPTITORQUE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·Product code DQO·January 20, 2021