BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    PE-3000 PULSE RATE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209126873·

    ARGON LASER PHOTOCOAGULATOR SYS REPEAT MODE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    JAKOBI SURG. INSTRUMENTS #12 40/41

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·December 3, 2012

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Injury ·HEARTWARE, INC·Product code DSQ·June 6, 2014

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·September 30, 2010

    MENTOR SILTEX ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·December 7, 2018