BEUDAMED
    8 results · 27ms · 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.

    ADVANCED MICRO-OSMOMETER MODEL 3300

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DRILL SLEEVE F. SOLID STEPDRILL

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·February 23, 2012

    LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    [CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TI DISTRACTION LOCK

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MDI·June 6, 2017

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·February 14, 2013

    R3

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·January 17, 2011

    MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 28, 2014