Brand Name | CLEARLINK BLOOD RECIPIENT SET |
Type of Device | SET, BLOOD TRANSFUSION |
Manufacturer (Section D) |
BAXTER HEALTHCARE - DOMINICAN REPUBLIC |
haina, san cristobal |
|
Manufacturer (Section G) |
BAXTER HEALTHCARE - DOMINICAN REPUBLIC |
carretera sanchez km 18.5 |
parque industrial itabo, piisa |
haina, san cristobal |
DR
|
|
Manufacturer Contact |
|
25212 w. illinois route 120 |
round lake, IL 60073
|
2242702068
|
|
MDR Report Key | 7642030 |
MDR Text Key | 112892679 |
Report Number | 1416980-2018-03904 |
Device Sequence Number | 1 |
Product Code |
BRZ
|
UDI-Device Identifier | 00085412046341 |
UDI-Public | (01)00085412046341 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K993120 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,consum |
Reporter Occupation |
Other
|
Type of Report
| Initial,Followup |
Report Date |
07/27/2018 |
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
|
Device Operator |
Other
|
Device Expiration Date | 02/21/2023 |
Device Catalogue Number | 2C8750 |
Device Lot Number | DR18B20038 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
05/31/2018 |
Initial Date FDA Received | 06/27/2018 |
Supplement Dates Manufacturer Received | 07/03/2018
|
Supplement Dates FDA Received | 07/27/2018
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 02/21/2018 |
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
N
|
Patient Sequence Number | 1 |
|
|