MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-30 for BENEVISION CENTRAL MONITORING SYSTEM manufactured by Shenzhen Mindray Bio-medical Electronics Co., Ltd.
Report Number | 2221819-2020-00002 |
MDR Report Key | 9649188 |
Date Received | 2020-01-30 |
Date of Report | 2020-01-06 |
Date of Event | 2020-01-04 |
Date Facility Aware | 2020-01-06 |
Report Date | 2020-01-30 |
Date Reported to Mfgr | 2020-01-30 |
Date Added to Maude | 2020-01-30 |
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 | BIOMEDICAL ENGINEER |
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 | BENEVISION CENTRAL MONITORING SYSTEM |
Generic Name | BENEVISION |
Product Code | MSX |
Date Received | 2020-01-30 |
Model Number | BENEVISION CENTRAL MONITORING SYSTEM |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD |
Manufacturer Address | 1203 NANHUAN AVENUE GUANGMING GUANGMING DISTRICT SHENZHEN, 518106 CH 518106 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-30 |