International safety notice
Information concerning the modification of software version 4.29 and the renal replacement therapy device Octo Nova® of the company MeSys GmbH
Germany / BfArM · DEU · Aug 24, 2007
Key facts
| Title | Information concerning the modification of software version 4.29 and the renal replacement therapy device Octo Nova® of the company MeSys GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Information concerning the modification of software version 4.29 and the renal replacement therapy device Octo Nova® of the company MeSys GmbH |
| Manufacturer | Information concerning the modification of software version 4.29 and the renal replacement therapy device Octo Nova® of the company MeSys GmbH |
| Models | 0-20413, 30419, 1.3.ANOMALIES, 1.4.ANOMALLES, 1.1.DISPLAY, 1.2.LLMITATLON, «ANREDE_2», 5.ACTIVATION, GE-F076 |
| Date | Aug 24, 2007 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
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