| Brand Name | EEA |
| Common Device Name | STAPLER, SURGICAL |
| 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 | 50167803 |
| Report Number | 2647580-2026-02298 |
| Device Sequence Number | 5306158 |
| Product Code |
GAG
|
| UDI-Device Identifier | 10884523004731 |
| UDI-Public | (01)10884523004731(17)301231(10)P6A0942S(20)01 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | CH |
| PMA/510(K) Number | K221003 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Device Implanted Year | 2026 |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Foreign,Health Professional,Company Representative |
| Initial Reporter Occupation |
Other Health Care Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
08/06/2026 |
| 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 | EEA25 |
| Device Catalogue Number | EEA25 |
| Device Lot Number | P6A0942S |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
Yes
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 07/23/2026 |
| Initial Report FDA Received Date | 08/06/2026 |
| Date Device Manufactured | 01/09/2026 |
| 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 | 65 YR |
| Patient Sex | Female |
| Patient Weight | 123 LB |