| Brand Name | EXACTAMIX |
| Common Device Name | Set, i.V. Fluid transfer |
| Manufacturer (Section D) |
| BAXTER HEALTHCARE CORPORATION |
| deerfield IL |
|
| Manufacturer (Section G) |
| ECM - PLASTICOS Y MATERIAS PRIMAS PYMPSA - SP013600 |
| 3609-2 juan de la barrera |
| parque industrial el alamo |
| guadalajara, jalisco NA 44490 |
|
MX
44490
|
|
| Manufacturer Contact |
|
|
| 25212 w. illinois route 120 |
| round lake, IL 60073
|
|
+1(224)270-5355
|
|
| MDR Report Key | 50923573 |
| Report Number | 1416980-2026-03043 |
| Device Sequence Number | 5803970 |
| Product Code |
LHI
|
| UDI-Device Identifier | 00085412475790 |
| UDI-Public | (01)00085412475790(10)804086(17)280922 |
| Combination Product (Y/N) | N |
| Initial Reporter State | NA |
| Initial Reporter Country | UK |
| PMA/510(K) Number | K002705 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Foreign,User Facility,Company Representative |
| Type of Report
| Initial |
| Report Date (Section B) |
09/28/2026 |
| 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 | H938174 |
| Device Catalogue Number | H938174 |
| Device Lot Number | 804086 |
| 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 | 09/01/2026 |
| Initial Report FDA Received Date | 09/28/2026 |
| 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 |
|
|