MAUDE report
MAUDE report 7231: MIYA HOOK
Malfunction · received Oct 14, 1993 · SHERIDAN CATHETER CORPORATION
Key facts
| MDR report key | 7231 |
|---|---|
| Report number | 2024347-1993-09001 |
| Event type | Malfunction |
| Brand name | MIYA HOOK |
| Catalog number | 433-142 |
| Manufacturer | SHERIDAN CATHETER CORPORATION |
| Product code | FHB |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Oct 14, 1993 |
| Report date | Nov 18, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1–9 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: