MAUDE report
MAUDE report 15989: ZOLL PD 1200
Malfunction · received Jul 21, 1994 · ZMI CORPORATION
Key facts
| MDR report key | 15989 |
|---|---|
| Report number | 15989 |
| Event type | Malfunction |
| Brand name | ZOLL PD 1200 |
| Model number | PD 1200 |
| Manufacturer | ZMI CORPORATION |
| Product code | DRK |
| Device class | Class III |
| Date received by FDA | Jul 21, 1994 |
| Report date | Apr 11, 1994 |
| Report source | Maude |
At a glance
- None Device problems coded
- 100–999 MAUDE reports for this product code
- 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: