BEUDAMED
    7 results · 18ms · 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 ×

    GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE

    FDA 510(k)

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613025755·Lister Bandage Scissors, Angled, Probe Tip, Two...

    OPTOS ADVANCE

    FDA 510(k)
    FDA Class 2 ·Radiology

    SILMED NASAL SEPTAL BUTTON

    FDA 510(k)
    FDA Unclassified ·Unknown

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 14, 2013

    ALLEGRETTO WAVE

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code LZS·November 12, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 3, 2014