MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-08-26 for ICS IMPULSE, 1085 8-04-16217 manufactured by Natus Medical Denmark Aps (gn Otometrics).
| Report Number | 9612197-2019-00007 |
| MDR Report Key | 8930492 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2019-08-26 |
| Date of Report | 2019-09-23 |
| Date of Event | 2019-07-31 |
| Date Mfgr Received | 2019-08-01 |
| Device Manufacturer Date | 2017-09-20 |
| Date Added to Maude | 2019-08-26 |
| 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 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MISS LOUISE CALLANAN |
| Manufacturer Street | HOERSKAETTEN 9 |
| Manufacturer City | TAASTRUP, 2630 |
| Manufacturer Country | DA |
| Manufacturer Postal | 2630 |
| Manufacturer G1 | NATUS MEDICAL DENMARK (GN OTOMETRICS) |
| Manufacturer Street | IDA BUSINESS PARK GORT |
| Manufacturer City | GALWAY, CONNAUGHT H91PD92 |
| Manufacturer Country | DA |
| Manufacturer Postal Code | H91PD92 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ICS IMPULSE, 1085 |
| Generic Name | ICS IMPULSE, 1085 |
| Product Code | GWN |
| Date Received | 2019-08-26 |
| Returned To Mfg | 2019-08-15 |
| Model Number | 8-04-16217 |
| Catalog Number | 8-04-16217 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | NATUS MEDICAL DENMARK APS (GN OTOMETRICS) |
| Manufacturer Address | HOERSKAETTEN 9, TAASTRUP, 2630 DA 2630 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-08-26 |