BEUDAMED
    7 results · 26ms · 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.

    NTI-1000

    FDA 510(k)
    FDA Class 2 ·Neurology

    SCEPTOR PSEUDOMONAS PLUS MIC/ID PANEL

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CANMED 103 9300 ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Neurology

    ADVANCE 35 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Injury ·COOK, INC.·Product code LIT·June 20, 2014

    PLUS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC·Product code HSD·November 9, 2010

    2520274-2013-00035

    FDA Adverse Event
    Injury ·SYNTHES·Product code MJO·January 3, 2013

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020