MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2012-09-10 for PANASONIC'S MCO-18AC CO2 INCUBATOR * manufactured by Panasonic Corp Of North America.
Report Number | 2820316 |
MDR Report Key | 2820316 |
Date Received | 2012-09-10 |
Date of Report | 2012-09-10 |
Date of Event | 2012-09-05 |
Report Date | 2012-09-10 |
Date Reported to FDA | 2012-09-10 |
Date Added to Maude | 2012-11-06 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PANASONIC'S MCO-18AC CO2 INCUBATOR |
Generic Name | BATH, INCUBATORS/WATER, CO2 |
Product Code | JTQ |
Date Received | 2012-09-10 |
Model Number | MCO-18AC |
Catalog Number | * |
Lot Number | * |
ID Number | * |
Operator | OTHER |
Device Availability | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PANASONIC CORP OF NORTH AMERICA |
Manufacturer Address | ONE PANASONIC WAY SECAUCUS NJ 07094 US 07094 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2012-09-10 |