BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    MILLIPORE DUAL RATE INTRAVENOUS CASSETTE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ERA® Micro 11° DO Small Post Female SS

    FDA UDI
    STERNGOLD DENTAL LLC·00841549101977·This part contains: 1 female, 2 black, 2 white,...

    EVOLVE (R) TRIAD (TM) PLATING SYSTEM AND EVOLVE (R) TRIAD (TM) BONE SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ProVectra 3D Prime with VistaSoft

    FDA 510(k)
    FDA Class 2 ·Radiology

    ENSEAL G2 ARTICULATING

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·May 15, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·October 31, 2012

    4 MOTOR ADVANCE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·August 17, 2010

    OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial Components (Product Line: 02-012-38-XXXX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

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