MAUDE report
MAUDE report 42741: STORZ ONE-PIECE POSTERIOR CHAMBER LENS
Other · received Oct 16, 1996 · STORZ OPHTHALMICS, INC.
Key facts
| MDR report key | 42741 |
|---|---|
| Report number | 1119279-1996-00012 |
| Event type | Other |
| Brand name | STORZ ONE-PIECE POSTERIOR CHAMBER LENS |
| Model number | P336UV |
| Catalog number | P366UV |
| Manufacturer | STORZ OPHTHALMICS, INC. |
| Product code | HQL |
| Device class | Class III |
| Date received by FDA | Oct 16, 1996 |
| Report date | Oct 15, 1996 |
| 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: