MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-11-08 for NICOLET EEG GROUP 842-693200 manufactured by Natus Neuro Incorporated.
Report Number | 3010611950-2019-00065 |
MDR Report Key | 9296660 |
Report Source | USER FACILITY |
Date Received | 2019-11-08 |
Date of Report | 2019-10-10 |
Date of Event | 2019-10-10 |
Date Mfgr Received | 2019-10-10 |
Date Added to Maude | 2019-11-08 |
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 | MS. JANESSA BOONE |
Manufacturer Street | 3150 PLEASANT VIEW ROAD |
Manufacturer City | MIDDLETON WI 53562 |
Manufacturer Country | US |
Manufacturer Postal | 53562 |
Manufacturer Phone | 6088298603 |
Manufacturer G1 | NATUS NEUROLOGY INCORPORATED |
Manufacturer Street | 3150 PLEASANT VIEW ROAD |
Manufacturer City | MIDDLETON WI 53562 |
Manufacturer Country | US |
Manufacturer Postal Code | 53562 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NICOLET EEG GROUP |
Generic Name | VIDEO CART MONOPOD DOME CAMERA |
Product Code | GWQ |
Date Received | 2019-11-08 |
Returned To Mfg | 2019-10-22 |
Model Number | 842-693200 |
Catalog Number | 842-693200 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | NATUS NEURO INCORPORATED |
Manufacturer Address | 3150 PLEASANT VIEW ROAD MIDDLETON WI 53562 US 53562 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-11-08 |