MAUDE manufacturer profile
MEDTRONIC NEUROMODULATION · MAJ
MAUDE profile for Catheter, Percutaneous, Intraspinal, Short Term
Key facts
| Manufacturer | MEDTRONIC NEUROMODULATION |
|---|---|
| Manufacturer group | MEDTRONIC NEUROMODULATION |
| Product code | MAJ |
| Product code name | Catheter, Percutaneous, Intraspinal, Short Term |
At a glance
- 10–99 MAUDE reports
- 1–9 Injury reports
- 1–9 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Adverse Event Without Identified Device or Use Problem, Perforation of Vessels, Hemorrhage/Blood Loss/Bleeding, No Known Impact Or Consequence To Patient, Difficult to Advance, Material Integrity Problem, Headache, Lumbar Puncture, Tingling Most reported problems
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE manufacturer and product code profiles
Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.
Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1