| Brand Name | Endo GIA Ultra |
| Common Device Name | STAPLE, IMPLANTABLE |
| Manufacturer (Section D) |
| Covidien |
| sabanetas industrial park |
| ponce PR 00716 -440 |
|
| Manufacturer (Section G) |
| Covidien |
| sabanetas industrial park |
|
| ponce PR 00716 -440 |
|
| Manufacturer Contact |
|
mike
bocchino
|
| 8200 coral sea st ne |
| mounds view, MN 55112--439
|
|
+1(800)646-4633
|
|
| MDR Report Key | 50745305 |
| Report Number | 2647580-2026-02652 |
| Device Sequence Number | 18733809 |
| Product Code |
GDW
|
| UDI-Device Identifier | 10884523003543 |
| UDI-Public | (01)10884523003543(17)300531(10)P5F1136S(20)01 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | US |
| PMA/510(K) Number | K111825 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Other,Foreign,Health Professional,Company Representative |
| Type of Report
| Initial,Followup |
| Report Date (Section B) |
09/28/2026 |
| 1 Device was Involved in the Event |
|
| 1 Patient was Involved in the Event |
|
| Is this an Adverse Event Report? |
No
|
| Is this a Product Problem Report? |
Yes
|
| Operator of Device |
Health Professional
|
| Device Model Number | EGIAUSTND |
| Device Catalogue Number | EGIAUSTND |
| Device Lot Number | P5F1136S |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
No
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 08/14/2026 |
| Supplement Date Received by Manufacturer | 09/25/2026
|
| Initial Report FDA Received Date | 09/12/2026 |
| Supplement Report FDA Received Date | 09/28/2026
|
| Date Device Manufactured | 06/25/2025 |
| Is the Device Labeled for Single Use? (Y/N) |
Yes
|
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Usage of Device |
Initial
|
| Patient Sequence Number | 1 |
| Patient Age | 67 YR |
| Patient Sex | Male |
|
|