MAUDE report
MAUDE report 18065: CARDIAC PACEMAKERS, INCORPORATED
No Answer Provided · received Sep 13, 1994 · CARDIAC PACEMAKERS, INCORPORATED
Key facts
| MDR report key | 18065 |
|---|---|
| Report number | 18065 |
| Event type | No Answer Provided |
| Brand name | CARDIAC PACEMAKERS, INCORPORATED |
| Model number | UNKNOWN |
| Manufacturer | CARDIAC PACEMAKERS, INCORPORATED |
| Date received by FDA | Sep 13, 1994 |
| Report date | Dec 22, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- None 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: