| Brand Name | REPEATER |
| Common Device Name | Set, i.V. Fluid transfer |
| Manufacturer (Section D) |
| BAXTER HEALTHCARE CORPORATION |
| deerfield IL |
|
| Manufacturer (Section G) |
| ECM - AVAILMED S.A. DE C.V. - SP021332 |
| c. industrial lt. 001 mz. 105 |
| no 20905 int a, col cd ind. |
| tijuana, baja california NA 22444 |
|
MX
22444
|
|
| Manufacturer Contact |
|
|
| 25212 w. illinois route 120 |
| round lake, IL 60073
|
|
+1(224)270-5355
|
|
| MDR Report Key | 50747677 |
| Report Number | 1416980-2026-02943 |
| Device Sequence Number | 15565749 |
| Product Code |
LHI
|
| UDI-Device Identifier | 00085412475721 |
| Combination Product (Y/N) | N |
| Initial Reporter State | NA |
| Initial Reporter Country | TW |
| PMA/510(K) Number | NA |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Foreign,Health Professional,Company Representative |
| Initial Reporter Occupation |
Other Health Care Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
09/13/2026 |
| 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 |
Other
|
| Device Model Number | H93811 |
| Device Catalogue Number | H93811 |
| Device Lot Number | 60707303 |
| 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 | 08/17/2026 |
| Initial Report FDA Received Date | 09/13/2026 |
| 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 |
|
|