BEUDAMED
    7 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.

    MODEL 6888 LEAD TUNNELER

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    MODEL 366-14 INTERMEDICS LEAD CONNECTOR CAP

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SPARTAN SOLDER

    FDA 510(k)
    FDA Class 2 ·Dental

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·April 18, 2018

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 21, 2014

    DEPUY ASR XL FEM IMP SIZE 39

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 3, 2013

    U BY KOTEX CLICK TAMPONS

    FDA Adverse Event
    Malfunction ·QINGDAO P AND B CORP LTD·Product code HEB·November 5, 2010