BEUDAMED
    10 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.

    SMART BURS TOTAL CARBIDES

    FDA 510(k)
    FDA Class 1 ·Dental

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110966·STERILIZING CASE 4-KNIVES

    Grasping forceps

    FDA UDI
    SOPRO-COMEG GmbH·04059082022703·

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·August 28, 2020

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 26, 2024

    GAM-200

    FDA 510(k)
    FDA Class 2 ·Dental

    LASERPRO 16

    FDA 510(k)
    FDA Class 2 ·Radiology

    GORE INTRODUCER SHEATH WITH SILICONE PINCH VALVE

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCAITES·Product code DYB·January 10, 2013

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·December 10, 2010

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 8, 2014