MAUDE report
MAUDE report 13777: ORGANAN TEKNIKA
Injury · received May 10, 1994 · C/G/H
Key facts
| MDR report key | 13777 |
|---|---|
| Report number | 2243621-1994-05079 |
| Event type | Injury |
| Brand name | ORGANAN TEKNIKA |
| Model number | BIO MODERATE |
| Catalog number | 0170100 |
| Manufacturer | C/G/H |
| Product code | KDI |
| Device class | Class II |
| Date received by FDA | May 10, 1994 |
| Report date | Apr 20, 1994 |
| 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: