BEUDAMED
    9 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 ×

    Xenix Medical Sacroiliac Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MILAGRO

    FDA UDI
    Medos International Sàrl·10886705022335·MILAGRO ADVANCE INTERFERENCE SCREW Absorbable -...

    HEMOSIL FACTOR IX DEFICIENT PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    INTELLIVUE PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SENSOR ENLITE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·November 6, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 1, 2011

    CONQUEST PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·July 12, 2013

    ARCOS 17X150MM SPL TPR DIST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 12, 2024

    ARCOS CON SZ C STD 60MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 12, 2024