International safety notice
Information for the Software RenalSoft Observational Study v.2.0, RenalSoft v.1.1 and Renal Software Suite v.3.1 HD-Modul (Renal Link), Baxter
Germany / BfArM · DEU · Jun 16, 2006
Key facts
| Title | Information for the Software RenalSoft Observational Study v.2.0, RenalSoft v.1.1 and Renal Software Suite v.3.1 HD-Modul (Renal Link), Baxter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Software RenalSoft Observational Study v.2.0, RenalSoft v.1.1 and Renal Software Suite v.3.1 HD-Modul (Renal Link), Baxter |
| Manufacturer | Information for the Software RenalSoft Observational Study v.2.0, RenalSoft v.1.1 and Renal Software Suite v.3.1 HD-Modul (Renal Link), Baxter |
| Models | GA-01, 203044, 875794, EDMOÜ1E, W142J, V.2.0, 05.2005, V.3.1, 234.5, L800-553, SYSTERN1000, 01.DD and 4 more |
| Date | Jun 16, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1