MAUDE report
MAUDE report 3927: AVI MODEL 1610 BURETTE IV ADMINISTRATION SET
Malfunction · received Jul 31, 1992 · AVI, INC. 3M HEALTH CARE
Key facts
| MDR report key | 3927 |
|---|---|
| Report number | 3927 |
| Event type | Malfunction |
| Brand name | AVI MODEL 1610 BURETTE IV ADMINISTRATION SET |
| Model number | 1610 |
| Catalog number | 1610 |
| Manufacturer | AVI, INC. 3M HEALTH CARE |
| Product code | FPA |
| Device class | Class II |
| Date received by FDA | Jul 31, 1992 |
| Report date | Apr 1, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 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: