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    Modulus Inc.

    FDA registration
    Modulus Inc.·1 product·🇺🇸 United States

    MODULUS DATA SYSTEMS, INC.

    FDA registration
    MODULUS DATA SYSTEMS, INC.·1 product·🇺🇸 United States

    UNK - CAGE/SPACER: PEEK

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL CH·Product code MAX·April 11, 2022

    UNK - CAGE/SPACER: PEEK

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL CH·Product code MAX·April 11, 2022

    BARDEX LUBRI-SIL ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·October 13, 2020

    BARDEX® ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·April 14, 2020

    BARDEX® LUBRI-SIL® ALL-SILICONE TEMP SENSING FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·December 3, 2019

    BARDEX® ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GBM·April 6, 2022

    BARDEX ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·July 22, 2020

    BARDEX LUBRICATH FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·September 4, 2020

    BARDEX® ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·April 2, 2020

    BARDEX® LUBRI-SIL® ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·August 10, 2021

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code KNW·June 2, 2006

    TERUMO PERFUSION SYSTEM 8000

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·March 7, 2014

    TERUMO CDI 101 MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTY·March 14, 2011

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DTQ·July 1, 2011

    POWERLED

    FDA Adverse Event
    Malfunction ·MAQUET S.A.·Product code FSY·June 25, 2015

    TERUMO CENTRIFUGAL SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWA·July 22, 2010

    HEARTSTART MRX MONITOR/DEFIB

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code MKJ·July 27, 2021

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·January 24, 2021