| Primary Device ID | 15694311111146 |
| NIH Device Record Key | f971bfa0-ed43-430d-aaa1-9255763b7882 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nox C1 Kit |
| Version Model Number | NOX-C1KIT1 |
| Catalog Number | 544020 |
| Company DUNS | 365741462 |
| Company Name | Nox Medical ehf. |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 9999999999 |
| support@noxmedical.com | |
| Phone | 9999999999 |
| support@noxmedical.com | |
| Phone | 9999999999 |
| support@noxmedical.com | |
| Phone | 9999999999 |
| support@noxmedical.com | |
| Phone | 9999999999 |
| support@noxmedical.com | |
| Phone | 9999999999 |
| support@noxmedical.com | |
| Phone | 9999999999 |
| support@noxmedical.com | |
| Phone | 9999999999 |
| support@noxmedical.com | |
| Phone | 9999999999 |
| support@noxmedical.com | |
| Phone | 9999999999 |
| support@noxmedical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 15694311111146 [Primary] |
| OLZ | Automatic Event Detection Software For Polysomnograph With Electroencephalograph |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-03-03 |
| Device Publish Date | 2020-02-24 |
| 15694311111146 | NOX-C1KIT1 |
| 15694311111504 | NOX-C1KIT1_US |