BEUDAMED
    7 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 ×

    Endosee System

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306804823·Frazier Suction Tube, 9fr

    EXELO2, MODEL 4010

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

    ENDOWRIST ONE VESSEL SEALER

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

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·July 29, 2011

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 6, 2008

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·June 26, 2013