International safety notice
Follow-up Information for IMMULITE/IMMULITE 1000 Androstenedione, Siemens Healthcare Diagnostics Inc.
Germany / BfArM · DEU · Jan 6, 2015
Key facts
| Title | Follow-up Information for IMMULITE/IMMULITE 1000 Androstenedione, Siemens Healthcare Diagnostics Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | IMMULITE/IMMULITE 1000 Androstenedione, Siemens Healthcare Diagnostics Inc. |
| Manufacturer | Follow-up Information for IMMULITE/IMMULITE 1000 Androstenedione, Siemens Healthcare Diagnostics Inc. |
| Models | 0.4303, 0.967, 0.352, LKAO1, 0.095, 0.513, 40850, 0.791, 40270, 0.537, 0.300, 0.064 and 34 more |
| Date | Jan 6, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 100–999 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