MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,l report with the FDA on 2019-07-02 for UNKNOWN IMPLANTABLE NEUROSTIMULATOR NEU_INS_STIMULATOR manufactured by Medtronic Neuromodulation.
Report Number | 3007566237-2019-01469 |
MDR Report Key | 8755773 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,L |
Date Received | 2019-07-02 |
Date of Report | 2019-07-02 |
Date of Event | 2019-02-11 |
Date Mfgr Received | 2019-06-04 |
Date Added to Maude | 2019-07-02 |
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 | UNKNOWN IMPLANTABLE NEUROSTIMULATOR |
Generic Name | IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS) |
Product Code | MRU |
Date Received | 2019-07-02 |
Model Number | NEU_INS_STIMULATOR |
Catalog Number | NEU_INS_STIMULATOR |
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. Required No Informationntervention | 2019-07-02 |