BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    BLUE LUXCER CURING LIGHT, MODELS M-830, M-835 AND M-855

    FDA 510(k)
    FDA Class 2 ·Dental

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70606461·Sprint II Bracket Roth .018" 20 Brackets 3-5 w....

    AT HOME DRUG TEST, MODEL 9083 T

    FDA 510(k)
    FDA Unclassified ·Unknown

    DISPOSABLE INJECTOR OR DISPOSABLE SCLEROTHERAPY NEEDLE

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

    TERUMO TCM II COOLING AND HEATING SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP·Product code DWC·April 5, 2013

    RESTORE RECHARGEABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·June 13, 2008

    4.0 CANN.CANCEL LAG 42MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HWC·April 6, 2011

    EDWARDS LOCKING SYRINGE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code MAV·June 16, 2023

    EDWARDS LOCKING SYRINGE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES LLC·Product code MAV·March 29, 2022