MAUDE report
MAUDE report 46190: PD2000 ADVISORY
Malfunction · received Oct 23, 1996 · ZOLL MEDICAL, CORP.
Key facts
| MDR report key | 46190 |
|---|---|
| Report number | 1220908-1996-00062 |
| Event type | Malfunction |
| Brand name | PD2000 ADVISORY |
| Model number | PD2000 |
| Catalog number | PD2000 |
| Manufacturer | ZOLL MEDICAL, CORP. |
| Product code | MKJ |
| Device class | Class III |
| Date received by FDA | Oct 23, 1996 |
| Report date | Oct 23, 1996 |
| 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
- None Injury reports for this brand
- 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: