BEUDAMED
    7 results · 23ms · 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 ×

    LACTATE DEHYDROGENASE (LD) TEST ITEM #65418

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BC-1201 CAST ABUTMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    F383 RECHARGEABLE MINI MASSAGER

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    PROGRESSA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 25, 2014

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 22, 2013

    UNICEL® DXC 600 PRO SYNCHRON® CHEMISTRY ANALYZER

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code JJE·December 14, 2010

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021