MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2020-03-10 for ROCHE 9180 ELECTROLYTE ANALYZER ISE 9180 03157334001 manufactured by Roche Diagnostics.
Report Number | 1823260-2020-00700 |
MDR Report Key | 9813123 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2020-03-10 |
Date of Report | 2020-04-02 |
Date of Event | 2020-02-20 |
Date Mfgr Received | 2020-02-20 |
Date Added to Maude | 2020-03-10 |
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 | NA MICHAEL LESLIE |
Manufacturer Street | 9115 HAGUE ROAD NA |
Manufacturer City | INDIANAPOLIS IN 46250 |
Manufacturer Country | US |
Manufacturer Postal | 46250 |
Manufacturer Phone | 3175214343 |
Manufacturer G1 | ROCHE INSTRUMENT CENTER AG TEGIMENTA |
Manufacturer Street | FORRENSTRASSE NA |
Manufacturer City | ROTKREUZ 6343 |
Manufacturer Country | SZ |
Manufacturer Postal Code | 6343 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ROCHE 9180 ELECTROLYTE ANALYZER |
Generic Name | ELECTROLYTE ANALYZER |
Product Code | JFP |
Date Received | 2020-03-10 |
Model Number | ISE 9180 |
Catalog Number | 03157334001 |
Lot Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ROCHE DIAGNOSTICS |
Manufacturer Address | 9115 HAGUE ROAD INDIANAPOLIS IN 462500457 US 462500457 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-10 |