BEUDAMED
    9 results · 19ms · 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 ×

    KARL STORZ TELE-SCRUB

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ROCHE REAGENT FOR CHLORIDE, FOR THE COBAS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Fusion Craniofacial Implant; Fusion Skull Implant

    FDA 510(k)
    FDA Class 2 ·Neurology

    STRATA II UNISHUNT, SMALL

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·February 6, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 6, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 22, 2014

    11.0MM TI HELICAL BLADE 95MM

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HSB·July 22, 2016

    LARGE EX-FIX 11MM CRBN FBR ROD 250MM / MR-CONDITIONAL

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018

    LARGE EX-FIX 11MM CRBN FBR ROD 300MM / MR-CONDITIONAL

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018