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.

    VITEK RAPID CALL-GRAM POSITIVE IDENTIFICATION CARD

    FDA 510(k)
    FDA Class 1 ·Microbiology

    VOYAGR SERIES DIAGNOSTIC EP CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BARD MARLEX MESH DART

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ENDOLOOP LIGATURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GEA·December 27, 2018

    SHARPS CONTAINER

    FDA Adverse Event
    Malfunction ·POST MEDICAL, INC.·Product code FMI·March 12, 2024

    COULTER® LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·January 22, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014