Brand Name | ARCHITECT HBSAG QUALITATIVE II CONFIRMATORY REAGENT KIT |
Type of Device | TEST, HEPATITIS B (B CORE, BE ANTIGEN, BE ANTIBODY, B CORE IGM) |
Manufacturer (Section D) |
ABBOTT IRELAND |
finisklin business park |
sligo F91VY 44 |
EI F91VY44 |
|
Manufacturer (Section G) |
ABBOTT IRELAND |
finisklin business park |
|
sligo F91VY 44 |
EI
F91VY44
|
|
Manufacturer Contact |
siobhan
wright
|
lisnamuck |
post market surveillance |
longford N39 E-932
|
EI
N39 E932
|
433331157
|
|
MDR Report Key | 16462236 |
MDR Text Key | 310460611 |
Report Number | 3008344661-2023-00044 |
Device Sequence Number | 1 |
Product Code |
LOM
|
Combination Product (y/n) | N |
Reporter Country Code | SP |
PMA/PMN Number | P110029 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial,Followup |
Report Date |
04/11/2023 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 03/01/2023 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 07/26/2023 |
Device Catalogue Number | 02G23-25 |
Device Lot Number | 43193FN00 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 04/05/2023 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 09/07/2022 |
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |
Treatment | ARC I2000SR RECONDIT SP, 03M74-96, (B)(6); ARC I2000SR RECONDIT SP, 03M74-96, (B)(6) |