MAUDE report
MAUDE report 3066: BARD LUBRICATH 18 FRENCH 30CC BALLOON
Injury · received Jul 27, 1992 · BARD UROLOGICAL DIVISION
Key facts
| MDR report key | 3066 |
|---|---|
| Report number | 3066 |
| Event type | Injury |
| Brand name | BARD LUBRICATH 18 FRENCH 30CC BALLOON |
| Model number | 0166 L18 |
| Catalog number | UNKNOWN |
| Manufacturer | BARD UROLOGICAL DIVISION |
| Product code | GBA |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Jul 27, 1992 |
| Report date | May 22, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 100–999 MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- 1–9 Injury reports for this brand
- 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: