BEUDAMED
    6 results · 33ms · 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.

    MINI POLYURETHANE CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACS 0.015 & 0.018 PRESSURE GUIDE WIRE W/MICRO.

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Tigon Medical Tissue Anchors

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·February 26, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·February 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 6, 2014