MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2005-09-21 for COMMANDER XG RMT-RTC2K UNK manufactured by Resonance Technolgies, Inc..
[21960957]
Pt undergoing mri lumbar spine on ge 1. 5t excite system while wearing resonance technologies cinema vision goggles complained of heating to face at point of contact with vision goggles fifteen minutes into examination. Goggles were removed for remainder of exam.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1036661 |
| MDR Report Key | 735500 |
| Date Received | 2005-09-21 |
| Date of Report | 2005-09-20 |
| Date of Event | 2005-09-06 |
| Date Added to Maude | 2006-07-19 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | COMMANDER XG |
| Generic Name | CINEMA VISION |
| Product Code | HOY |
| Date Received | 2005-09-21 |
| Model Number | RMT-RTC2K |
| Catalog Number | UNK |
| Lot Number | NA |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | * |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 723390 |
| Manufacturer | RESONANCE TECHNOLGIES, INC. |
| Manufacturer Address | * NORTHRIDGE CA * US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2005-09-21 |