MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-02-20 for TOPCO 87-736-001 manufactured by Sejoy Electronics & Instruments Co, Ltd.
Report Number | 1422443-2020-00002 |
MDR Report Key | 9734840 |
Date Received | 2020-02-20 |
Date of Report | 2020-02-20 |
Date of Event | 2020-01-18 |
Date Facility Aware | 2020-01-20 |
Report Date | 2020-02-20 |
Date Reported to FDA | 2020-02-20 |
Date Reported to Mfgr | 2020-02-20 |
Date Added to Maude | 2020-02-20 |
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 |
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 | TOPCO |
Generic Name | 10-SECOND FLEXIBLE TIP THERMOMETER |
Product Code | FLL |
Date Received | 2020-02-20 |
Model Number | 87-736-001 |
Catalog Number | 87-736-001 |
Lot Number | 5977600119627 |
Operator | LAY USER/PATIENT |
Device Availability | Y |
Device Age | 12 MO |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SEJOY ELECTRONICS & INSTRUMENTS CO, LTD |
Manufacturer Address | BLDG 2, NO.202, ZHENZHONG ROAD WEST LAKE ECONOMY & TECH ZONE HANGZHOU, 310030 CH 310030 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization | 2020-02-20 |