BEUDAMED
    30 results · 24ms · Sources: EU EUDAMED, US FDA

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    FUJI IP CASSETTE TYPE PC

    FDA 510(k)
    FDA Class 2 ·Radiology

    E310 OTP Cuspidor Delivery System

    FDA UDI
    Engle Dental Systems, LLC·00850043433279·Utility Center Mounted Dr. & Asst E300 Cuspidor...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587P07092070·7mm PLIF Implant 9mm Wide 20mm Length, 7 deg Lo...

    TRANSDUCERS FOR FETAL ULTRASONIC AND TOKODYNAMOMETER MONITORING

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    REAADS IGA ANTI-PHOSPHATIDYLSERINE SEMI-QUANTITATIVE TEST KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 26, 2025

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·April 22, 2013

    ENDO GIA ROTICULATOR 45-3.5 SULU

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GDW·April 19, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·ANIMAS CORP·Product code LZG·July 7, 2008

    COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 18, 2017

    AMERITUS TEMPERATURE PROBE

    FDA Adverse Event
    Injury ·KENTEC MEDICAL, INC·Product code FMT·October 29, 2020

    CABLE CERCLAGE CABLE WITH CRIMP 1.8 MM DIA. 635 MM LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KTT·September 18, 2018

    COMPREHENSIVE REVERSE SHOULDER CENTRAL SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 18, 2017

    VNGD SSK PS TIB BRG 10X71/75

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 18, 2018

    VG 360 DST FM AG 67.5X5 LL/RM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 18, 2018

    COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE MINI BASEPLATE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·September 6, 2017

    ABBOTT TUBE EDTA PLH 13X75 2.0 PNK

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·August 3, 2022

    ABBOTT TUBE EDTA PLH 13X75 2.0 PNK

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·September 17, 2019

    VG 360 DST FM AG 67.5X5 RL/LM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 18, 2018

    VG 360 DST FM AG 67.5X15 LL/RM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 18, 2018