MAUDE report
MAUDE report 26886: DUAL EFFECT BARE LASER FIBER
Malfunction · received Sep 22, 1995 · LASER INDUSTRIES, LTD.
Key facts
| MDR report key | 26886 |
|---|---|
| Report number | 8010121-1995-00002 |
| Event type | Malfunction |
| Brand name | DUAL EFFECT BARE LASER FIBER |
| Model number | 600 MICRON DUAL EFFECT FIBER |
| Catalog number | AA2214000 |
| Manufacturer | LASER INDUSTRIES, LTD. |
| Product code | LLO |
| Device class | Class II |
| Date received by FDA | Sep 22, 1995 |
| Report date | Sep 22, 1995 |
| Report source | Maude |
At a glance
- None Device problems coded
- 10–99 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: