MAUDE report
MAUDE report 59737: DUAL LINE CUSTOMER KIT
Malfunction · received Dec 23, 1996 · OHMEDA (S) PTE LTD
Key facts
| MDR report key | 59737 |
|---|---|
| Report number | 8020616-1996-00007 |
| Event type | Malfunction |
| Brand name | DUAL LINE CUSTOMER KIT |
| Model number | PMKITT IDT-XX ROSE |
| Catalog number | PMKIT IDT-XX ROSE |
| Manufacturer | OHMEDA (S) PTE LTD |
| Product code | DRS |
| Device class | Class II |
| Date received by FDA | Dec 23, 1996 |
| Report date | Dec 17, 1996 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None 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: