BEUDAMED
    8 results · 28ms · 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 ×

    ACE BROOKER BONE PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASAHI GAIA FIRST, SECOND, THIRD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IDEIA PCE CHLAMYDIA

    FDA 510(k)
    FDA Class 1 ·Microbiology

    WALLSTENT ENDOSPROSTHESIS WITH UNISTEP PLUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code FGE·November 20, 2006

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·May 27, 2014

    RUSCH CARLENS ENDOBRONCHIAL TUBE, 39F

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTS·November 5, 2012

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWP·June 10, 2015

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015