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.
[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
Report Number | 2221819-2020-00006 |
MDR Report Key | 9901044 |
Date Received | 2020-03-30 |
Date of Report | 2020-02-28 |
Date of Event | 2020-02-21 |
Date Facility Aware | 2020-02-28 |
Report Date | 2020-03-26 |
Date Reported to FDA | 2020-03-26 |
Date Reported to Mfgr | 2020-03-26 |
Date Added to Maude | 2020-03-30 |
Event Key | 0 |
Report Source Code | Distributor report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | GAS MODULE 3 |
Generic Name | GAS MODULE |
Product Code | BZK |
Date Received | 2020-03-30 |
Catalog Number | 0998-00-1900-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD |
Manufacturer Address | BUILDINGS 9-13 BAIWANGXIN HIGH-TECH INDUSTRIAL PARK BAIMANG, XILI TOWN, NANSHAN, SHENZEN 518108 CH 518108 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Death | 2020-03-30 |