MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2017-08-18 for NURO 3533 manufactured by Medtronic Neuromodulation.
[83093452]
Patient Sequence No: 1, Text Type: N, H10
[83093453]
The patient reported that they were on medication for a urinary tract infection. It was indicated that the patient was on maintenance sessions with the next session scheduled for (b)(6) 2017. There were no further complications reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3007566237-2017-03376 |
MDR Report Key | 6805354 |
Report Source | CONSUMER |
Date Received | 2017-08-18 |
Date of Report | 2017-08-18 |
Date Mfgr Received | 2017-08-15 |
Date Added to Maude | 2017-08-18 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | LISA WOODWARD CLARK |
Manufacturer Street | 7000 CENTRAL AVENUE NE RCW215 |
Manufacturer City | MINNEAPOLIS MN 55432 |
Manufacturer Country | US |
Manufacturer Postal | 55432 |
Manufacturer Phone | 7635263920 |
Manufacturer G1 | MEDTRONIC NEUROMODULATION |
Manufacturer Street | 800 53RD AVE NE |
Manufacturer City | MINNEAPOLIS MN 554211200 |
Manufacturer Country | US |
Manufacturer Postal Code | 554211200 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NURO |
Generic Name | STIMULATOR,PERIPHERAL NERVE,NON-IMPLANTED,FOR PELVIC FLOOR DYSFUNCTION |
Product Code | NAM |
Date Received | 2017-08-18 |
Model Number | 3533 |
Catalog Number | 3533 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC NEUROMODULATION |
Manufacturer Address | 800 53RD AVE NE MINNEAPOLIS MN 554211200 US 554211200 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2017-08-18 |