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.

    DURAFLOR

    FDA 510(k)
    FDA Class 2 ·Dental

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471130500·K-WIRE - DOUBLE TROCAR WITH GUIDE 0.9mm DIA x 1...

    AR1000 SERIES ULTRASONIC WOUND THERAPY SYSTEM

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

    MODIFICATION TO TRANSPORT INCUBATOR 185

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 28, 2013

    PUMP MMT-523RNAP PRDGM INS V2.3 PL EN RC

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·December 8, 2010

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·July 14, 2014