BEUDAMED
    7 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.

    ALEXANDER MANUFACTURING RECHARGEABLE BATTERY (M1/T)

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

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970799·anteriors; shade D3 light; mould UBIM

    MODULARIS VARIOSTAR

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

    AP 50/30 Insufflator with Insuflow Port

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

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 29, 2014

    COOLFLOW® IRRIGATION PUMP

    FDA Adverse Event
    Malfunction ·HEI, INC.·Product code DRF·February 20, 2013

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code MMI·January 25, 2011