MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2007-01-02 for MORCHER 1-L * manufactured by Morcher.
[549866]
Fixation suture erosion through conjunctiva in ctr study eye. Not device related. Patch graft placed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1041489 |
| MDR Report Key | 800811 |
| Date Received | 2007-01-02 |
| Date of Report | 2006-12-27 |
| Date of Event | 2006-12-27 |
| Date Added to Maude | 2007-01-08 |
| Event Key | 0 |
| Report Source Code | Voluntary 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 | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MORCHER |
| Generic Name | CTR - 1L |
| Product Code | MRJ |
| Date Received | 2007-01-02 |
| Model Number | 1-L |
| Catalog Number | * |
| Lot Number | AEMAJA |
| ID Number | * |
| Device Availability | N |
| Device Age | * |
| Implant Flag | Y |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 788350 |
| Manufacturer | MORCHER |
| Manufacturer Address | * * * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2007-01-02 |