BEUDAMED
    7 results · 21ms · 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.

    KILEJIAN CIRCUMCISION TEMPLATE [THE DOME]

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    STRYKER 5000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PEDICRAGT BASSINET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UNK

    FDA Adverse Event
    Injury ·Product code FTR·February 1, 2013

    ADVANTA

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·December 28, 2010

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 21, 2014

    HARMONIC SCALPEL HANDPIECES (EXACT CODE UNKNOWN)

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 26, 2019