BEUDAMED
    6 results · 27ms · 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 ×

    OMNI-VENT, SERIES D

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    URINARY DRAINAGE BAG 2D9017

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301

    FDA 510(k)
    FDA Unclassified ·Unknown

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 13, 2014

    PORTEX 6.0MM VOCALAID TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INT'L, LTD·Product code BTO·October 11, 2010

    SETROX S 45

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·December 4, 2012