MAUDE report
MAUDE report 747: UNKNOWN
Injury · received Jun 22, 1992 · MIDMARK CORP, RITTER MEDICAL PRODUCTS
Key facts
| MDR report key | 747 |
|---|---|
| Report number | 747 |
| Event type | Injury |
| Brand name | UNKNOWN |
| Model number | 100L |
| Catalog number | THE RITTER 100 SERIES |
| Manufacturer | MIDMARK CORP, RITTER MEDICAL PRODUCTS |
| Product code | LGX |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Jun 22, 1992 |
| Report date | Apr 15, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 10–99 MAUDE reports for this product code
- 1,000+ MAUDE reports for this brand
- 100–999 Death reports for this brand
- 1,000+ Injury reports for this brand
- Yes Adverse event flagged
- No 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: