| Brand Name | VasoView Hemopro 2 |
| Common Device Name | Electrosurgical, Cutting & Coagulation & Accessories |
| Manufacturer (Section D) |
| Maquet Cardiovascular LLC |
| 45 barbour pond drive |
| wayne NJ 07470 |
|
| Manufacturer (Section G) |
| Maquet Cardiovascular LLC |
| 45 barbour pond drive |
|
| wayne NJ 07470 |
|
| Manufacturer Contact |
|
arelean
guzman
|
| 45 barbour pond drive |
| wayne, NJ 07470
|
|
| MDR Report Key | 50794921 |
| Report Number | 2242352-2026-0000809 |
| Device Sequence Number | 16084429 |
| Product Code |
GEI
|
| UDI-Device Identifier | 00607567700406 |
| UDI-Public | (01)00607567700406(10)3000562996(17)280520 |
| Combination Product (Y/N) | N |
| Initial Reporter State | FL |
| Initial Reporter Country | US |
| PMA/510(K) Number | K101274 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Health Professional,User Facility,Company Representative |
| Initial Reporter Occupation |
Nurse
|
| Type of Report
| Initial |
| Report Date (Section B) |
09/16/2026 |
| 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 | VH-4000 |
| Device Catalogue Number | VH-4000 |
| Device Lot Number | 3000562996 |
| Is the Reporter a Health Professional? |
Yes
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 08/25/2026 |
| Initial Report FDA Received Date | 09/16/2026 |
| Date Device Manufactured | 05/21/2026 |
| Is the Device Labeled for Single Use? (Y/N) |
Yes
|
| Usage of Device |
Initial
|
| Patient Sequence Number | 1 |
| Patient Age | 71 YR |
| Patient Sex | Male |
| Patient Weight | 187 LB |