BEUDAMED
    6 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.

    MQL 20 ND:YAG OPHTHALMIC LASER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ADAP-TEMP, MODEL: AT-100

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TITMUS VISION TESTER II

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·June 19, 2014

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORP·Product code LZG·October 25, 2010

    DEPUY ASR XL FEM IMP SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 24, 2012