BEUDAMED
    9 results · 25ms · 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.

    CARESIDE CKMB

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 8, 2006

    BECE PRESS

    FDA 510(k)
    FDA Class 2 ·Dental

    EMS 300 MUSCLE STIMULATORS

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MOBILE FLUOROSCOPIC IMAGE INTENSIFIED SYSTEM

    FDA Adverse Event
    Malfunction ·OEC MEDICAL SYSTEMS·Product code JAA·January 9, 1997

    TRIDENT 0 DEG CONSTRAINED INSERT 22D

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWZ·March 5, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    ATTAIN OTW

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWP·August 7, 2014

    MENTOR SMOOTH ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·October 14, 2020