MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-11-18 for ARCHITECT HBSAG QUALITATIVE II CONFIRMATORY 02G23-25 manufactured by Abbott Ireland.
Report Number | 3008344661-2019-00133 |
MDR Report Key | 9335168 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-11-18 |
Date of Report | 2019-11-18 |
Date of Event | 2019-10-17 |
Date Mfgr Received | 2019-10-31 |
Date Added to Maude | 2019-11-18 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | CHRISTIAN LEE |
Manufacturer Street | 100 ABBOTT PARK ROAD DEPT 09B9, BLDG CP01-3 |
Manufacturer City | ABBOTT PARK IL 600643537 |
Manufacturer Country | US |
Manufacturer Postal | 600643537 |
Manufacturer Phone | 224668-294 |
Manufacturer G1 | ABBOTT IRELAND |
Manufacturer Street | DIAGNOSTICS DIVISION FINISKLIN BUSINESS PARK |
Manufacturer City | SLIGO NA |
Manufacturer Country | EI |
Manufacturer Postal Code | NA |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ARCHITECT HBSAG QUALITATIVE II CONFIRMATORY |
Generic Name | HBSAG CONFIRMATORY |
Product Code | KSJ |
Date Received | 2019-11-18 |
Catalog Number | 02G23-25 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ABBOTT IRELAND |
Manufacturer Address | DIAGNOSTICS DIVISION FINISKLIN BUSINESS PARK SLIGO NA EI NA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-18 |