International safety notice
Field Safety Notice from Johnson & Johnson Medical GmbH for implantable infusion pump model Archimedes
Germany / BfArM · DEU · Nov 12, 2008
Key facts
| Title | Field Safety Notice from Johnson & Johnson Medical GmbH for implantable infusion pump model Archimedes |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | implantable infusion pump model Archimedes |
| Manufacturer | Field Safety Notice from Johnson & Johnson Medical GmbH for implantable infusion pump model Archimedes |
| Models | 22844, 28443550, 97-43, D-22806, 97-01, 1045NO |
| Date | Nov 12, 2008 |
| 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