BEUDAMED
    3 results · 21ms · 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 FDA Adverse Event ×

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 11, 2013

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code DTB·January 10, 2011

    11.0MM TI HELICAL BLADE 100MM

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HSB·July 23, 2014