BEUDAMED
    10 results · 35ms · 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.

    LIQUICHEK ANA CONTROL, EIA SCREEN, MODEL 205

    FDA 510(k)
    FDA Class 2 ·Immunology

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984473·anteriors; shade C2; mould Q 83

    LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    RUBIN BONE PLANER W/REPLACEABLE BLADE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    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

    RIATA ACTIVE FIXATION

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

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 27, 2011

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·August 6, 2014

    DAILIES TOTAL 1

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