MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-20 for BAUSCH AND LOMB CRYSTALENS manufactured by Bausch And Lomb Inc.
| Report Number | MW5087513 |
| MDR Report Key | 8722793 |
| Date Received | 2019-06-20 |
| Date of Report | 2019-06-20 |
| Date Added to Maude | 2019-06-21 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | BAUSCH AND LOMB CRYSTALENS |
| Generic Name | LENS, INTRAOCULAR, ACCOMODATIVE |
| Product Code | NAA |
| Date Received | 2019-06-20 |
| Device Availability | * |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BAUSCH AND LOMB INC |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-06-20 |