MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-09 for GE COROMETRICS NAUTILUS 2264LAX TOCO TRANSDUCER WITH WING FFCM3260 manufactured by Ge Healthcare.
Report Number | 3007409280-2019-00001 |
MDR Report Key | 8773666 |
Date Received | 2019-07-09 |
Date of Report | 2016-03-07 |
Date of Event | 2016-03-07 |
Date Mfgr Received | 2016-03-07 |
Date Added to Maude | 2019-07-09 |
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 | BIOMEDICAL ENGINEER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | JENNA VARGAS |
Manufacturer Street | 212 AVENIDA FABRICANTE |
Manufacturer City | SAN CLEMENTE CA 92672 |
Manufacturer Country | US |
Manufacturer Postal | 92672 |
Manufacturer G1 | AVANTE HEALTH SOLUTIONS |
Manufacturer Street | 212 AVENIDA FABRICANTE |
Manufacturer City | SAN CLEMENTE CA 92672 |
Manufacturer Country | US |
Manufacturer Postal Code | 92672 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | GE COROMETRICS NAUTILUS 2264LAX TOCO TRANSDUCER WITH WING |
Generic Name | TOCOTRANSDUCER |
Product Code | HGM |
Date Received | 2019-07-09 |
Returned To Mfg | 2016-03-18 |
Model Number | 2264LAX |
Catalog Number | FFCM3260 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | GE HEALTHCARE |
Manufacturer Address | 8880 GORMAN RD LAUREL MD 20723 US 20723 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-07-09 |