BEUDAMED
    7 results · 19ms · 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 ×

    LC MICROHYBRID

    FDA 510(k)
    FDA Class 2 ·Dental

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984484·anteriors; shade C2; mould 93

    AUDIOTESTER SCREENING AUDIOMETER

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MAGNETIC RESONANCE DIAGNOSTIC HELMHOLTZ NECK COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013

    TILDA R 53 US

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVN·August 6, 2014

    DEXTRUS 4135

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·February 1, 2011