International safety notice
Information for System 1000 and Arena Hemodialysis Instruments, Baxter
Germany / BfArM · DEU · Mar 12, 2009
Key facts
| Title | Information for System 1000 and Arena Hemodialysis Instruments, Baxter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | System 1000 and Arena Hemodialysis Instruments, Baxter |
| Manufacturer | Information for System 1000 and Arena Hemodialysis Instruments, Baxter |
| Models | S10003TD, 502-402, 31701-330, 85716, 42976, S10003T, 09193, 157-1278-946, 85701, 31701-361, SIOOOL3TD |
| Date | Mar 12, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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