BEUDAMED
    10 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.

    VRS 3 WALL STAND

    FDA 510(k)
    FDA Class 1 ·Radiology

    STAXX FX SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VuePoint OCT System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 23, 2014

    UNICEL® DXI 800 ACCESS® IMMUNOASSAY ANALYZER

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code JLW·January 8, 2011

    VERSYS FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LPH·February 25, 2016

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·SYNTHES BETTLACH·Product code LXH·August 17, 2015

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·July 14, 2023

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·December 1, 2021