MAUDE report
MAUDE report 16127: SURGICAL LASER TECHNOLOGIES
Malfunction · received Jul 21, 1994 · SURGICAL LASER TECHNOLOIES, INCORPORATED
Key facts
| MDR report key | 16127 |
|---|---|
| Report number | 16127 |
| Event type | Malfunction |
| Brand name | SURGICAL LASER TECHNOLOGIES |
| Catalog number | MTR 1.5 |
| Manufacturer | SURGICAL LASER TECHNOLOIES, INCORPORATED |
| Date received by FDA | Jul 21, 1994 |
| Report date | May 24, 1994 |
| Report source | Maude |
At a glance
- None Device problems coded
- 10–99 MAUDE reports for this brand
- None Death reports for this brand
- 1–9 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: