Primary Device ID | 00863609000341 |
NIH Device Record Key | 9c93a075-fbf1-441b-b9b9-4503b15ce349 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Eko Mobile App Android |
Version Model Number | 1.2.9 |
Company DUNS | 079670921 |
Company Name | EKO DEVICES, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
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 |
---|---|
GS1 | 00863609000341 [Primary] |
OUG | Medical Device Data System |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-11-08 |
Device Publish Date | 2018-08-16 |
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