BEUDAMED
    8 results · 19ms · 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 ×

    SEPACELL(R) R-200/500 LEUKOCYTE REMOVAL RECIP SETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD PLASTIPAK 50ML CONCENTRIC LUER LOCK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 28, 2019

    ON-SITE ALCOHOL

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    VACUUM ERECTION DEVICE (VED)

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

    BD VACUTAINER BRAND NEEDLES

    FDA Adverse Event
    Malfunction ·BD·Product code FMI·November 15, 2010

    ROTALINK¿ PLUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code MCX·January 9, 2013

    UNIFY ASSURA DR CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·July 1, 2014

    TFN-ADVANCED Proximal Femoral Nailing System (TFNA); for treatment of fractures in orthopedics and trauma.

    FDA Enforcement
    Class II ·Terminated·Synthes, Inc.·May 20, 2015