MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2018-06-13 for EEG-1200A manufactured by Nihon Kohden Corporation.
[111150806]
The biomedical engineer reported that the ups started smoking during the use of the eeg-1200a. The unit was in use on patients at the time, but no patient harm was reported. Nihon kohden will submit a supplemental report in accordance with 21 cfr section 803. 56 if additional information becomes available.
Patient Sequence No: 1, Text Type: N, H10
[111150807]
The biomedical engineer reported that the ups started smoking during the use of the eeg-1200a.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 8030229-2018-00207 |
| MDR Report Key | 7598830 |
| Report Source | USER FACILITY |
| Date Received | 2018-06-13 |
| Date of Report | 2018-06-13 |
| Date of Event | 2018-05-15 |
| Date Facility Aware | 2018-05-15 |
| Report Date | 2018-06-13 |
| Date Reported to FDA | 2018-06-13 |
| Date Reported to Mfgr | 2018-06-13 |
| Date Mfgr Received | 2018-06-13 |
| Date Added to Maude | 2018-06-13 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | BIOMEDICAL ENGINEER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | SHAMA MOOMAN |
| Manufacturer Street | SAFETY MGMT DEPT, QUALITY MGMT SEIBU BLDG 2, 4TH FLOOR 1-11-2 |
| Manufacturer City | KUSUNOKIDAI TOKOROZAWA, SAITAMA 359-8580 |
| Manufacturer Country | JA |
| Manufacturer Postal | 359-8580 |
| Manufacturer G1 | NIHON KOHDEN TOMIOKA CORPORATION |
| Manufacturer Street | 1-1 TAJINO ATTN: SHAMA MOOMAN |
| Manufacturer City | TOMIOKA CITY, GUNMA 370-2314 |
| Manufacturer Country | JA |
| Manufacturer Postal Code | 370-2314 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | EEG-1200A |
| Generic Name | NEUROFAX ELECTROENCEPHALOGRAPH |
| Product Code | OLT |
| Date Received | 2018-06-13 |
| Model Number | EEG-1200A |
| Catalog Number | EEG-1200A |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Device Age | 0 MO |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | NIHON KOHDEN CORPORATION |
| Manufacturer Address | 1-31-4 NISHIOCHIA, SHINJUKU-KU ATTN: SHAMA MOOMAN TOKYO, 161-8560 JA 161-8560 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-06-13 |