GAS MODULE 3 0998-00-1900-01

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-30 for GAS MODULE 3 0998-00-1900-01 manufactured by Shenzhen Mindray Bio-medical Electronics Co., Ltd.

Event Text Entries

[185628694] The user facility requested an evaluation of the equipment; no malfunction of the equipment was claimed. The results of the evaluation determined the gas module required n2o calibration only.
Patient Sequence No: 1, Text Type: N, H10


[185628695] It was reported that a patient monitored on a passport 2 monitor and gas module was having surgery and one minute into the procedure the patient's heart stopped; the patient later expired.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2221819-2020-00006
MDR Report Key9901044
Date Received2020-03-30
Date of Report2020-02-28
Date of Event2020-02-21
Date Facility Aware2020-02-28
Report Date2020-03-26
Date Reported to FDA2020-03-26
Date Reported to Mfgr2020-03-26
Date Added to Maude2020-03-30
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGAS MODULE 3
Generic NameGAS MODULE
Product CodeBZK
Date Received2020-03-30
Catalog Number0998-00-1900-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerSHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD
Manufacturer AddressBUILDINGS 9-13 BAIWANGXIN HIGH-TECH INDUSTRIAL PARK BAIMANG, XILI TOWN, NANSHAN, SHENZEN 518108 CH 518108


Patients

Patient NumberTreatmentOutcomeDate
101. Death 2020-03-30

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