MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-02-28 for MCKESSON 159-003 manufactured by Suzhou Meccan Imp.& Exp Co.,.
| Report Number | 1314417-2020-00013 |
| MDR Report Key | 9770521 |
| Date Received | 2020-02-28 |
| Date of Report | 2020-02-28 |
| Date of Event | 2020-01-29 |
| Date Added to Maude | 2020-02-28 |
| 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 | MCKESSON |
| Generic Name | LARYNGEAL MASK |
| Product Code | CAE |
| Date Received | 2020-02-28 |
| Model Number | 159-003 |
| Lot Number | 20180701 |
| Device Availability | * |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SUZHOU MECCAN IMP.& EXP CO., |
| Manufacturer Address | 12 EAST CHUNSHEN LAKE ROAD XIANGCHENG DISTRICT SUZHOU, CHINA US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-02-28 |