MAUDE report
MAUDE report 6363: PRECISION MEDICAL CHROMEBODY FLOWMETER
Malfunction · received Aug 31, 1993 · PRECISION MEDICAL, INC.
Key facts
| MDR report key | 6363 |
|---|---|
| Report number | 6363 |
| Event type | Malfunction |
| Brand name | PRECISION MEDICAL CHROMEBODY FLOWMETER |
| Model number | IMFA 1001 |
| Catalog number | IMFA 1001 |
| Manufacturer | PRECISION MEDICAL, INC. |
| Product code | ETL |
| Date received by FDA | Aug 31, 1993 |
| Report date | Aug 4, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1–9 MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- None Injury reports for this brand
- No 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: