MAUDE report
MAUDE report 25493: KELMAN AC 21 IOL
Injury · received Aug 8, 1995 · ALLERGAN MEDICAL OPTICS
Key facts
| MDR report key | 25493 |
|---|---|
| Report number | 25493 |
| Event type | Injury |
| Brand name | KELMAN AC 21 IOL |
| Model number | KELMAN AC 21 |
| Manufacturer | ALLERGAN MEDICAL OPTICS |
| Product code | HQL |
| Device class | Class III |
| Date received by FDA | Aug 8, 1995 |
| Report date | Mar 14, 1995 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- 1–9 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: