BEUDAMED
    11 results · 23ms · Sources: EU EUDAMED, US FDA

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    Genesys Spine Apache Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Walgreens

    FDA UDI
    WALGREEN CO.·00311917142067·Walgreens Gauze Pad. 3 IN X 3 IN.

    PD CATH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    APEX POINTER+; MEASRUING CABLE, HOOK, LIP CLIP, TOUCH PROBE (ACCESSORIES)

    FDA 510(k)
    FDA Unclassified ·Unknown

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·March 3, 2005

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·December 10, 2020

    GMK SPHERE TIBIAL TRAY FIXED CEMENTED SIZE T4-I3 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 20, 2018

    CARELINK

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·June 8, 2013

    POLYFLUX LR CAPILLARY DIALYZER

    FDA Adverse Event
    Malfunction ·GAMBRO DIALYSATOREN GMBH·Product code MSF·September 4, 2008

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·June 17, 2011

    FUSION 8MM-40CM UNSUPP PERIPHERAL GRAFT

    FDA Adverse Event
    Malfunction ·MAQUET CV·Product code DSY·February 8, 2017