MAUDE report
MAUDE report 50865: TEGWIRE BALLOON DILATION CATHETER
Malfunction · received Sep 19, 1996 · MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP.
Key facts
| MDR report key | 50865 |
|---|---|
| Report number | 1219544-1996-00046 |
| Event type | Malfunction |
| Brand name | TEGWIRE BALLOON DILATION CATHETER |
| Catalog number | 11-209 |
| Manufacturer | MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP. |
| Product code | LIT |
| Device class | Class II |
| Date received by FDA | Sep 19, 1996 |
| Report date | Aug 23, 1996 |
| 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
- 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: