| Brand Name | HERCULES 3 STAGE WIREGUIDED BALLOON ESOPHAGEAL-PYLORIC-COLONIC |
| Common Device Name | DILATOR, ESOPHAGEAL |
| Manufacturer (Section D) |
| WILSON-COOK MEDICAL INC (COOK ENDOSCOPY) |
| 4900 bethania station rd |
| winston salem NC 27105 |
|
| Manufacturer (Section G) |
| WILSON-COOK MEDICAL INC (COOK ENDOSCOPY) |
| 4900 bethania station rd |
|
| winston salem NC 27105 |
|
| Manufacturer Contact |
|
sabrina
o'brien
|
| 4900 bethania station rd |
| winston salem, NC 27105
|
|
3367440157
|
|
| MDR Report Key | 25812647 |
| Report Number | 1037905-2026-00345 |
| Device Sequence Number | 14940690 |
| Product Code |
KNQ
|
| UDI-Device Identifier | 00827002517967 |
| UDI-Public | (01)00827002517967(17)290227(10)W5011340 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | CL |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Foreign,Company Representative,Distributor |
| Initial Reporter Occupation |
Non-Healthcare Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
07/14/2026 |
| 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 | G51796 |
| Device Catalogue Number | HBD-W-12-13.5-15 |
| Device Lot Number | W5011340 |
| Was Device Available for Evaluation? |
No
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 06/17/2026 |
| Initial Report FDA Received Date | 07/14/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| Date Device Manufactured | 02/27/2026 |
| Is the Device Labeled for Single Use? (Y/N) |
Yes
|
| Usage of Device |
Initial
|
| Patient Sequence Number | 1 |
| Patient Age | 72 YR |
| Patient Sex | Female |