MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-10-23 for NIM? 2.0 MAINFRAME - PULSE 8252201 manufactured by Medtronic Xomed Inc..
Report Number | 1045254-2019-00533 |
MDR Report Key | 9224824 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-10-23 |
Date of Report | 2019-11-22 |
Date of Event | 2019-06-26 |
Date Mfgr Received | 2019-10-25 |
Device Manufacturer Date | 2006-04-17 |
Date Added to Maude | 2019-10-23 |
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 | CHRISTY CAIN |
Manufacturer Street | 6743 SOUTHPOINT DRIVE NORTH |
Manufacturer City | JACKSONVILLE FL 32216 |
Manufacturer Country | US |
Manufacturer Postal | 32216 |
Manufacturer Phone | 9043328353 |
Manufacturer G1 | MEDTRONIC XOMED INC. |
Manufacturer Street | 6743 SOUTHPOINT DR N |
Manufacturer City | JACKSONVILLE FL 32216 |
Manufacturer Country | US |
Manufacturer Postal Code | 32216 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NIM? 2.0 MAINFRAME - PULSE |
Generic Name | ELECTROMYOGRAPH, DIAGNOSTIC |
Product Code | IKN |
Date Received | 2019-10-23 |
Returned To Mfg | 2019-11-11 |
Model Number | 8252201 |
Catalog Number | 8252201 |
Lot Number | 44082600 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC XOMED INC. |
Manufacturer Address | 6743 SOUTHPOINT DR N JACKSONVILLE FL 32216 US 32216 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-10-23 |