BEUDAMED
    13 results · 21ms · 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 ×

    DATES-OHMEDA AESTIVA SMARTVENT MRI

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993410·anteriors; shade C4; mould IM

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198215·AK3 PS Insert Trial Size 4, 10mm

    Child Malleable Blade

    FDA UDI
    KOROS U.S.A., INC.·10840199542908·Child Malleable Blade Size 1-1/2 x 4-3/4"

    AUTOSUTURE ENDO GIA SINGLE USE BLACK RELOAD WITH TRI-STAPLE TECHNOLOGY

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

    SOZO Body Fluid Analyzer

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 19, 2016

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·April 9, 2015

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·March 7, 2013

    EXPRESS LD ILIAC/BILIARY PREMOUNTED STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIO·February 16, 2011

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·August 8, 2014

    G7 PPS LTD ACET SHELL 50D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·October 30, 2020

    G7 VIT E NEUTRAL LNR 36MM D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 4, 2020