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.
    Filters Regulation: Us FDA ×

    Medifun Lancing Device, Model No. LD-E1

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

    3B LASER NEEDLE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    METHADONE METABOLITE (EDDP) ENZIME IMMUNOASSAY, CAT. NO. 190 (500 TEST KIT), NO. 191 (5000 TEST KIT)

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    UNKNOWN SOFRADIM PRODUCT

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·February 6, 2014

    ABC SCREW DRIVER F/SELF-LOCKING SCREWS

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code HXX·October 15, 2014

    TAXUS (TM) LIBERTÉ (TM)

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·September 1, 2011

    AMPHIRION DEEP PTA BALLOON CATHETER

    FDA Adverse Event
    Injury ·INVATEC SPA·Product code DQY·July 17, 2013

    Revogene, Catalog no. 610210. IVD test instrument

    FDA Enforcement
    Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022