BEUDAMED
    8 results · 20ms · 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 ×

    BB-613WP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319705735·Lucae Mallet 7-3/4" (19.4cm), 9oz. (265 grams) ...

    GELPOINT PATH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MITAKA UNIARM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code NZU·November 24, 2016

    PWRD ECH FLEX 60MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 26, 2013

    ARTHREX

    FDA Adverse Event
    Malfunction ·ARTHREX MED. INST. GMBH·Product code HRX·July 28, 2011

    MTOME ST HOLSTER/CABLES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code KNW·October 7, 2008