| Common Device Name | DETACHABLE ENDO POCKET |
| Manufacturer (Section D) |
| UNIMAX MEDICAL SYSTEMS INC. |
| 8f-2, no.127, lane 235, |
| pao chiao rd, xindian dist. |
| new taipei city, taiwan TW 23 1 |
| TW TW 231 |
|
| Manufacturer (Section G) |
| UNIMAX MEDICAL SYSTEMS INC. |
| 8f-2, no.127, lane 235, |
| pao chiao road, xindian dist. |
| new taipei city, 231 |
|
TW
231
|
|
| Manufacturer Contact |
|
kris
hsieh
|
| 8f-2, no.127, lane 235, |
| pao chiao road, xindian dist. |
| new taipei city, 231
|
|
TW
231
|
|
| MDR Report Key | 25572664 |
| Report Number | 3007791595-2026-00005 |
| Device Sequence Number | 5154780 |
| Product Code |
GCJ
|
| UDI-Device Identifier | 04714127860909 |
| UDI-Public | (01)04714127860909(17)300905(10)6252509154 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | US |
| PMA/510(K) Number | K103510 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Distributor |
| Initial Reporter Occupation |
Other
|
| Type of Report
| Initial |
| Report Date (Section B) |
06/22/2026 |
| 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
|
| Device Catalogue Number | SB979 |
| Device Lot Number | 6252509154 |
| Was Device Available for Evaluation? |
Yes
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | Not provided |
| Initial Report FDA Received Date | 06/21/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| 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 Sex | Unknown |
|
|