MAUDE report
MAUDE report 29619: LIGACLIP ERCA
Other · received Jan 10, 1996 · ETHICON ENDO SURGERY, INC.
Key facts
| MDR report key | 29619 |
|---|---|
| Report number | 29619 |
| Event type | Other |
| Brand name | LIGACLIP ERCA |
| Model number | ER 320 ERCA ML |
| Catalog number | H40T3J 2000-09 |
| Manufacturer | ETHICON ENDO SURGERY, INC. |
| Product code | GDO |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Jan 10, 1996 |
| Report date | Dec 5, 1995 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 10–99 MAUDE reports for this brand
- 1–9 Death reports for this brand
- 1–9 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: