MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-01-29 for ARCHITECT TOTAL T3 7K64-25 07K64-25 manufactured by A.i.d.d Longford.
Report Number | 3005094123-2020-00026 |
MDR Report Key | 9643156 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-01-29 |
Date of Report | 2020-01-29 |
Date Mfgr Received | 2020-01-22 |
Device Manufacturer Date | 2019-08-28 |
Date Added to Maude | 2020-01-29 |
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 | A.I.D.D LONGFORD |
Manufacturer Street | LISNAMUCK CO. LONGFORD |
Manufacturer City | LONGFORD NA |
Manufacturer Country | EI |
Manufacturer Postal Code | NA |
Single Use | 3 |
Remedial Action | NO |
Previous Use Code | 3 |
Removal Correction Number | 3005094123-10/22/18-001 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ARCHITECT TOTAL T3 |
Generic Name | TOTAL TRIIODOTHYRONINE |
Product Code | CDP |
Date Received | 2020-01-29 |
Model Number | 7K64-25 |
Catalog Number | 07K64-25 |
Lot Number | 06423UI00 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | A.I.D.D LONGFORD |
Manufacturer Address | LISNAMUCK CO. LONGFORD LONGFORD NA EI NA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-29 |