MAUDE report
MAUDE report 43622: MODIFIED C-LOOP POSTERIOR CHAMBER IOL
Injury · received Oct 18, 1996 · SURGIDEV CORPORATION
Key facts
| MDR report key | 43622 |
|---|---|
| Report number | 2020277-1996-00002 |
| Event type | Injury |
| Brand name | MODIFIED C-LOOP POSTERIOR CHAMBER IOL |
| Model number | 5.5BUV20-24 |
| Catalog number | 406U4 |
| Manufacturer | SURGIDEV CORPORATION |
| Product code | HQL |
| Device class | Class III |
| Date received by FDA | Oct 18, 1996 |
| Report date | Oct 16, 1996 |
| Report source | Maude |
At a glance
- None Device problems coded
- 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: