MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-01-13 for MASK SURGICAL SENSITIVE WHITE AT73335 manufactured by Quiroproductos De Cuauhtemoc S. De R.l. De C.v..
Report Number | 1423537-2020-00393 |
MDR Report Key | 9582374 |
Report Source | USER FACILITY |
Date Received | 2020-01-13 |
Date of Report | 2020-01-13 |
Date of Event | 2019-12-19 |
Date Mfgr Received | 2019-12-19 |
Date Added to Maude | 2020-01-13 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
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 |
Manufacturer Contact | PATRICIA TUCKER |
Manufacturer Street | 3651 BIRCHWOOD DRIVE |
Manufacturer City | WAUKEGAN IL 60085 |
Manufacturer Country | US |
Manufacturer Postal | 60085 |
Manufacturer Phone | 8478874151 |
Manufacturer G1 | QUIROPRODUCTOS DE CUAUHTEMOC S. DE R.L. DE C.V. |
Manufacturer Street | AVE. RIO STA. CLARA - LOTES 12 |
Manufacturer City | CUAUHTEMOC, CHIHUAHUA 31543 |
Manufacturer Country | MX |
Manufacturer Postal Code | 31543 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MASK SURGICAL SENSITIVE WHITE |
Generic Name | MASK, SURGICAL |
Product Code | FXX |
Date Received | 2020-01-13 |
Model Number | AT73335 |
Catalog Number | AT73335 |
Lot Number | 19EGH567 |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | QUIROPRODUCTOS DE CUAUHTEMOC S. DE R.L. DE C.V. |
Manufacturer Address | AVE. RIO STA. CLARA - LOTES 12 CUAUHTEMOC, CHIHUAHUA 31543 MX 31543 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-01-13 |