BEUDAMED
    6 results · 31ms · 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 ×

    RUSCH ULTRA TRACHEOFLEX FENESTRATED KIT CUFFED,UNCUFFED/ RUSCH TRACHEOFLEX TRACHEOSTOMY KIT UNCUFFED STERILE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NK PINCH SENSOR, MODEL PF002

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIFECARE PCA 3 V5.06

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code MEA·May 5, 2014

    UNKOWN STIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·February 15, 2013

    TRIATHLON TOTAL RIGHT KNEE REPLACEMENT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·January 11, 2011