MAUDE report
MAUDE report 29394: LIGACLIP MCA MULTIPLE CLIP APPLIER
Injury · received Dec 20, 1995 · ETHICON ENDO-SURGERY, INC.
Key facts
| MDR report key | 29394 |
|---|---|
| Report number | 29394 |
| Event type | Injury |
| Brand name | LIGACLIP MCA MULTIPLE CLIP APPLIER |
| Model number | MGM 20, MGL 20 |
| Catalog number | MGL 20(MED), MGL 20 (LGE) |
| Manufacturer | ETHICON ENDO-SURGERY, INC. |
| Product code | GDO |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Dec 20, 1995 |
| Report date | Dec 18, 1995 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 100–999 MAUDE reports for this brand
- 1–9 Death reports for this brand
- 1–9 Injury reports for this brand
- Yes 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: