BEUDAMED
    12 results · 32ms · 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.

    APO-SCREEN CALIBRATOR & CONTROL SET FOR HDL APO A1

    FDA 510(k)
    FDA Class 2 ·Immunology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209135233·

    ACTION-WHEELS & PLAY WHEELS

    FDA 510(k)

    KINNET

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    APPOSE ULC 35 REGULAR SKIN STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GDT·May 22, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 5, 2010

    TOTAL ASR FEM IMP SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·December 3, 2012

    PERI-GUARD PERICARDIUM WITH APEX PROCESSING

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·May 20, 2014

    PERI-GUARD PERICARDIUM WITH APEX PROCESSING

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·May 20, 2014

    PERI-GUARD PERICARDIUM WITH APEX PROCESSING

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·May 20, 2014

    PERI-GUARD PERICARDIUM WITH APEX PROCESSING

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·May 20, 2014

    PERI-GUARD PERICARDIUM WITH APEX PROCESSING

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·May 20, 2014