BEUDAMED
    10 results · 20ms · 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 ×

    DISPOSABLE ELECTROSURGERY GROUNDING PAD

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984276·anteriors; shade B2; mould O 52

    CADWELL FREEDOM EEG DEVICE

    FDA 510(k)
    FDA Class 2 ·Neurology

    BECKMAN KAPPA LIGHT CHAIN REAGENT

    FDA 510(k)
    FDA Class 2 ·Immunology

    DAILIES TOTAL 1

    FDA Adverse Event
    Injury ·CIBA VISION GMBH·Product code LPL·August 3, 2012

    DAILIES TOTAL 1

    FDA Adverse Event
    Injury ·CIBA VISION GMBH·Product code MVN·July 19, 2012

    DURATA STS OPTIM ACTIVE FIXATION

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

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·February 10, 2011

    TRIDENT PSL HA CLUSTER 58MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·August 6, 2014

    DAILIES TOTAL 1

    FDA Adverse Event
    Injury ·CIBA VISION GMBH·Product code MVN·November 9, 2012