International safety notice
Siemens is not aware of compatibility test for MR Scans with Tx/Rx Head MR Coil for Patients with Deep Brain Stimulation Implants
Germany / BfArM · DEU · Sep 8, 2005
Key facts
| Title | Siemens is not aware of compatibility test for MR Scans with Tx/Rx Head MR Coil for Patients with Deep Brain Stimulation Implants |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Patients with Deep Brain Stimulation Implants |
| Manufacturer | Siemens is not aware of compatibility test for MR Scans with Tx/Rx Head MR Coil for Patients with Deep Brain Stimulation Implants |
| Models | 60601-2-33, MR033, 12300, BERLIN-CHARI0TTENBURG, D-91050, 0-91052, 0-91050, D-91052, MR-OOO.896.38, 08.05, 09131 |
| Date | Sep 8, 2005 |
| 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