BEUDAMED
    7 results · 18ms · 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.

    ACUFLEX DISPOSABLE KNIVES

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    Ventura NanoMetalene System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981150785·Ventura NM Trial, 11mm x 20mm x 17mm

    PRECEPTIS TYMPANOSTOMY TUBE INSERTER

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    AMMONIA-L3K ASSAY, CATALOGUE NUMBER 233-10

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MINILINK TRANSMITTER

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·July 22, 2015

    ON-Q

    FDA Adverse Event
    Malfunction ·I-FLOW CORPORATION·Product code MEB·December 10, 2010

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·July 15, 2014