BERNOULLI MANAGEMENT SYSTEM 3274

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-28 for BERNOULLI MANAGEMENT SYSTEM 3274 manufactured by Mediana Co. Ltd..

Event Text Entries

[137816075] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[137816076] According to the reporter, the device had lost alarm volume and was not sounding. It was reported that the master volume was muted. The customer reported that there was no patient harm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2936999-2019-00150
MDR Report Key8378382
Date Received2019-02-28
Date of Report2019-02-28
Date of Event2019-01-30
Date Mfgr Received2019-01-31
Date Added to Maude2019-02-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactAVI KLUGER
Manufacturer Street5920 LONGBOW DRIVE
Manufacturer CityBOULDER CO 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone3035306582
Manufacturer G1MEDIANA CO. LTD.
Manufacturer Street1650 1 2 DONGHWA RI MUNMAK EU
Manufacturer CityKANGWON DO WONJU SI 00000
Manufacturer CountryKR
Manufacturer Postal Code00000
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBERNOULLI MANAGEMENT SYSTEM
Product CodeMSX
Date Received2019-02-28
Model Number3274
Catalog Number3274
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMEDIANA CO. LTD.
Manufacturer Address1650 1 2 DONGHWA RI MUNMAK EU KANGWON DO WONJU SI 00000 KR 00000


Patients

Patient NumberTreatmentOutcomeDate
10 2019-02-28

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