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 2020-03-30 for CELL-DYN RUBY ANALYZER 08H67-01 manufactured by Abbott Diagnostics Division.
Report Number | 2919069-2020-00010 |
MDR Report Key | 9899334 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2020-03-30 |
Date of Report | 2020-03-30 |
Date of Event | 2020-03-12 |
Date Mfgr Received | 2020-03-12 |
Date Added to Maude | 2020-03-30 |
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 DIAGNOSTICS DIVISION |
Manufacturer Street | 4551 GREAT AMERICA PARKWAY |
Manufacturer City | SANTA CLARA CA 95054 |
Manufacturer Country | US |
Manufacturer Postal Code | 95054 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CELL-DYN RUBY ANALYZER |
Generic Name | AUTOMATED HEMATOLOGY ANALYZER |
Product Code | GKZ |
Date Received | 2020-03-30 |
Model Number | 08H67-01 |
Catalog Number | 08H67-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ABBOTT DIAGNOSTICS DIVISION |
Manufacturer Address | 4551 GREAT AMERICA PARKWAY SANTA CLARA CA 95054 US 95054 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-30 |