BEUDAMED
    8 results · 17ms · 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 ×

    SYNTHES (USA) ARTICULATING DISTAL RADIUS (ADRF) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984498·anteriors; shade C3; mould O 48

    TROCHANTERIC NAIL KIT, TI GAMMA3 11X200MM X 125

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·November 7, 2012

    CROMATEST RHEUMATOID DIAGNOSTIC/RF LATEX TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    COTUBE LH IRMA ASSAY

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DURATA STS OPTIM PASSIVE FIXATION, DF4 CONNECTOR

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

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORP.·Product code LZG·February 1, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·August 6, 2014