LANTIS GE SATURN Adverse Event — Malfunction (MDR 2910081-2008-00011)
LANTIS GE SATURN Adverse Event — Malfunction (MDR 2910081-2008-00011) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LANTIS GE SATURN; Generic name: ACCELERATOR, LINEAR, MEDICAL; Manufacturer: IMPAC MEDICAL SYSTEM, INC..
| Device | LANTIS GE SATURN |
|---|---|
| Generic name | ACCELERATOR, LINEAR, MEDICAL |
| Manufacturer | IMPAC MEDICAL SYSTEM, INC. |
| Report number | 2910081-2008-00011 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-13 |
| Report source | Other, Company representation, Distributor, COMPANY REPRESENTATI |
| Source | openFDA MAUDE (device adverse events) |
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