MAUDE report
MAUDE report 28752: NEUROSIGN 100 NERVE MONITOR
Injury · received Nov 10, 1995 · THE MAGSTIM CO, LTD.
Key facts
| MDR report key | 28752 |
|---|---|
| Report number | 1037007-1995-00001 |
| Event type | Injury |
| Brand name | NEUROSIGN 100 NERVE MONITOR |
| Catalog number | 33-0700 |
| Manufacturer | THE MAGSTIM CO, LTD. |
| Product code | GZJ |
| Device class | Class II |
| Date received by FDA | Nov 10, 1995 |
| Report date | Nov 10, 1995 |
| Report source | Maude |
At a glance
- None Device problems coded
- 100–999 MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- 1–9 Injury reports for this brand
- Yes Adverse event flagged
- Yes Product problem flagged
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE medical device reports
MAUDE holds medical device reports (MDRs) of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by manufacturers, importers, user facilities and the public. A report alone does not establish that a device caused an event.
Source: U.S. Food and Drug Administration (FDA), MAUDE (Manufacturer and User Facility Device Experience) database · Source date: