| Brand Name | LIFESTREAM |
| Common Device Name | BALLOON EXPANDABLE VASCULAR COVERED STENT |
| Manufacturer (Section D) |
| CLEARSTREAM TECHNOLOGIES LTD. |
| moyne upper |
| enniscorthy, co. wexford N A |
| EI N A |
|
| Manufacturer (Section G) |
| CLEARSTREAM TECHNOLOGIES LTD. |
| moyne upper |
|
| enniscorthy, co. wexford N A |
|
EI
N A
|
|
| Manufacturer Contact |
|
michael
gaffney
|
| 800 w. rio salado pkwy |
| tempe, AZ 85281
|
|
4803032689
|
|
| MDR Report Key | 25867868 |
| Report Number | 9616666-2026-00174 |
| Device Sequence Number | 10640272 |
| Product Code |
PRL
|
| UDI-Device Identifier | 05391522081062 |
| UDI-Public | (01)05391522081062(17)290430(10)CMLS0081 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | JA |
| PMA/510(K) Number | P160024 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Other,Foreign,Company Representative |
| Initial Reporter Occupation |
Physician
|
| Type of Report
| Initial |
| Report Date (Section B) |
06/26/2026 |
| 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 Catalogue Number | LSMU1350637 |
| Device Lot Number | CMLS0081 |
| 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 | 06/24/2026 |
| Initial Report FDA Received Date | 07/19/2026 |
| 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 |