BEUDAMED
    8 results · 18ms · 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.

    RUBENOSTIKA(TM) IGM MICROELISA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ARTHREX MENISCAL DART, ARTHREX MENISCAL DARTSTICK, ARTHREX CHONDRAL DART

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    General Cutting Contra Handpiece

    FDA 510(k)
    FDA Class 1 ·Dental

    UNICEL® DXC 880I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·October 26, 2010

    ON-Q C BLOC: 400ML, 2-14ML/HR SELECT-A-FLOW

    FDA Adverse Event
    Malfunction ·I-FLOW, LLC·Product code MEB·December 18, 2012

    2520274-2013-10292

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code MNI·November 2, 2013

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·November 10, 2021

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·January 15, 2026