Brand Name | PLEXITRON SOLUTION ADMINISTRATION SETS |
Type of Device | SET, ADMINISTRATION, INTRAVASCULAR |
Manufacturer (Section D) |
BAXTER HEALTHCARE CORPORATION |
deerfield IL |
|
Manufacturer (Section G) |
BAXTER HEALTHCARE - CALI |
calle 36 no. 2c-22 |
apartado aero 2446 |
cali |
CO
|
|
Manufacturer Contact |
|
25212 w. illinois route 120 |
round lake, IL
|
2242702068
|
|
MDR Report Key | 12669714 |
MDR Text Key | 277683291 |
Report Number | 1416980-2021-06378 |
Device Sequence Number | 1 |
Product Code |
FPA
|
UDI-Device Identifier | 07707141305553 |
UDI-Public | (01)07707141305553 |
Combination Product (y/n) | Y |
Reporter Country Code | CO |
PMA/PMN Number | NA |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional,Company Representative |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial,Followup |
Report Date |
11/24/2021 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 10/20/2021 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Other
|
Device Catalogue Number | MRC0001MP |
Device Lot Number | SE21HA1 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 11/22/2021 |
Was Device Evaluated by Manufacturer? |
No
|
Date Device Manufactured | 08/21/2021 |
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |
Treatment | UNSPECIFIED SOLUTION; UNSPECIFIED SOLUTION |