MAUDE report
MAUDE report 59506: MULTIFIRE CLIP APPLIER AND TITANIUM CLIPS
Malfunction · received Dec 24, 1996 · AESCULAP AG
Key facts
| MDR report key | 59506 |
|---|---|
| Report number | 2916714-1996-00011 |
| Event type | Malfunction |
| Brand name | MULTIFIRE CLIP APPLIER AND TITANIUM CLIPS |
| Model number | * |
| Catalog number | PL506R, PL559T |
| Manufacturer | AESCULAP AG |
| Product code | GDO |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Dec 24, 1996 |
| Report date | Dec 24, 1996 |
| 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: