Primary Device ID | 05694110063021 |
NIH Device Record Key | fed18692-12d1-4098-8155-ccb46f93e823 |
Commercial Distribution Discontinuation | 2018-01-01 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Lifelines iEEG Portable Laptop System Wired |
Version Model Number | KHW1010 |
Company DUNS | 500793540 |
Company Name | Kvikna Medical ehf. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05694110063021 [Primary] |
OLT | Non-Normalizing Quantitative Electroencephalograph Software |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-18 |
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