| Primary Device ID | B006NVPUSB1 |
| NIH Device Record Key | 32f13815-47eb-48e5-93f0-d506428c1061 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nerveäna+® |
| Version Model Number | NONE |
| Company DUNS | 182057401 |
| Company Name | NEUROVISION MEDICAL PRODUCTS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B006NVPUSB1 [Primary] |
| HIBCC | NVPUSB1 [Package] Package: [1 Units] In Commercial Distribution |
| GWF | Stimulator, Electrical, Evoked Response |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-02-09 |
| Device Publish Date | 2024-02-01 |
| NVPIC6 | NONE |
| NVPFKITMFT5 | NONE |
| NVPFKITMF5 | NONE |
| NVPFKITMDT5 | NONE |
| NVPFKITMD5 | NONE |
| NVPTKITDCST5 | N/A |
| NVPTKITDCS5 | N/A |
| NVPTKITDCLT5 | N/A |
| NVPTKITDCL5 | N/A |
| NVPTKITC3P8T5 | N/A |
| NVPTKITC3P85 | N/A |
| NVPTKITC3P7T5 | N/A |
| NVPTKITC3P75 | N/A |
| NVPTKITC3P6T5 | N/A |
| NVPTKITC3P65 | N/A |
| B006NVPTST2 | N/A |
| B600NVPS2 | NONE |
| B600NVPMS2 | NONE |
| B006NVPUSB1 | NONE |
| NVPTKITDCSWF5 | NONE |
| NVPTKITDCSD5 | N/A |
| NVPTKITDCLWF5 | NONE |
| NVPTKITDCLD5 | N/A |
| NVPTKITC3P8WSF5 | N/A |
| NVPTKITC3P7WSF5 | N/A |
| B006NVPTKITC3P6WSF5 | N/A |
| B006NVPT1 | NONE |
| B006NVPSTST2 | NONE |
| B006NVPMK1 | NONE |