| Brand Name | Versaport |
| Common Device Name | LAPAROSCOPE, GENERAL & PLASTIC SURGERY |
| Manufacturer (Section D) |
| DAVIS & GECK CARIBE LTD |
| zona franca de san isidro |
| santo domingo 0101 |
| DR 0101 |
|
| Manufacturer (Section G) |
| DAVIS & GECK CARIBE LTD |
| zona franca de san isidro |
|
| santo domingo 0101 |
|
DR
0101
|
|
| Manufacturer Contact |
|
mike
bocchino
|
| 8200 coral sea st ne |
| mounds view, MN 55112--439
|
|
+1(800)646-4633
|
|
| MDR Report Key | 50129046 |
| Report Number | 9612501-2026-02141 |
| Device Sequence Number | 10528186 |
| Product Code |
GCJ
|
| UDI-Device Identifier | 10884521215399 |
| UDI-Public | (01)10884521215399(17)290331(10)J4D3362Y |
| Combination Product (Y/N) | N |
| Initial Reporter Country | MX |
| PMA/510(K) Number | K130435 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Foreign,Health Professional,Company Representative |
| Type of Report
| Initial |
| Report Date (Section B) |
08/04/2026 |
| 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 | UNVCA12STF |
| Device Catalogue Number | UNVCA12STF |
| Device Lot Number | J4D3362Y |
| 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 | 07/10/2026 |
| Initial Report FDA Received Date | 08/04/2026 |
| Date Device Manufactured | 04/12/2024 |
| 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 |