MAUDE report
MAUDE report 4273: AUTO SUTURE MULTIFIRE ENDO GIA 30
Malfunction · received Sep 25, 1992 · U.S. SURGICAL CORP.
Key facts
| MDR report key | 4273 |
|---|---|
| Report number | 4273 |
| Event type | Malfunction |
| Brand name | AUTO SUTURE MULTIFIRE ENDO GIA 30 |
| Model number | 030813 |
| Catalog number | 030813 |
| Manufacturer | U.S. SURGICAL CORP. |
| Product code | GAG |
| Device class | Class II |
| Date received by FDA | Sep 25, 1992 |
| Report date | Jun 15, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 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: