MAUDE report
MAUDE report 10003: TERUMO RADIFOCUS GUIDE WIRE M
No Answer Provided · received Jul 21, 1994 · MEDI-TECH (BOSTON SCIENTIFIC CORP.)
Key facts
| MDR report key | 10003 |
|---|---|
| Report number | 10003 |
| Event type | No Answer Provided |
| Brand name | TERUMO RADIFOCUS GUIDE WIRE M |
| Catalog number | 46-151 |
| Manufacturer | MEDI-TECH (BOSTON SCIENTIFIC CORP.) |
| Product code | DQX |
| Device class | Class II |
| Date received by FDA | Jul 21, 1994 |
| Report date | Jun 30, 1994 |
| 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
- None Injury reports for this brand
- 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: