BEUDAMED
    6 results · 27ms · 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.

    LEAP LE TEST KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER

    FDA 510(k)
    FDA Class 2 ·Radiology

    Sternal Closure System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN DEPUY SZ. 60 SECTOR CUP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.-1818910·Product code KWA·June 2, 2014

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·October 23, 2012

    CASPER

    FDA Adverse Event
    Malfunction ·AESCULAP·Product code JDW·September 17, 2010