Primary Device ID | 15694311111368 |
NIH Device Record Key | 6d8d8f9e-b929-4abe-82b6-c5f1c78425f2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Noxturnal PSG CD |
Version Model Number | NOX-NOXTPSG_CD |
Catalog Number | 539012 |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15694311111368 [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 |
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15694311111597 - Nox C1s Kit | 2021-07-19 |
15694311111467 - Nox T3s System | 2021-06-08 |
15694311110682 - Nox A1 Starter Sensor Kit, Adult | 2021-02-11 |