BEUDAMED
    7 results · 17ms · 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.

    CENTRIFUGES

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    VASCULAB BI-DIRECTIONAL DOPPLER, #D10

    FDA 510(k)
    FDA Class 2 ·Radiology

    TYPE I BRILLIANT INTRODUCER KIT, TYPE II BRILLIANT INTRODUCER KIT, TYPE III BRILLIANT INTRODUCER KIT, TYPE IV BRILLIANT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    10MM/130 DEG TI CANN TFNA 170MM - STERILE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·March 30, 2018

    XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·May 30, 2014

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·November 20, 2012

    CONCERTO CRT-D DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NIK·September 22, 2010