MAUDE report
MAUDE report 57005: FLO-GARD 6300 DUAL CHANNEL VOLUMETRIC INFUSION PUMP
Injury · received Dec 13, 1996 · BAXTER HEALTHCARE PTE. LTD.
Key facts
| MDR report key | 57005 |
|---|---|
| Report number | 6000001-1996-00351 |
| Event type | Injury |
| Brand name | FLO-GARD 6300 DUAL CHANNEL VOLUMETRIC INFUSION PUMP |
| Model number | 6300 |
| Catalog number | 2M8048 |
| Manufacturer | BAXTER HEALTHCARE PTE. LTD. |
| Product code | FRN |
| Device class | Class II |
| Date received by FDA | Dec 13, 1996 |
| Report date | Nov 14, 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
- None Death reports for this brand
- 1–9 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: