Primary Device ID | 00853553005318 |
NIH Device Record Key | a5587bbb-b59e-465e-91a1-b78406e94803 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Livongo Demo Kit |
Version Model Number | Livongo G2.0FW2.1 |
Catalog Number | KIT00803 |
Company DUNS | 829984561 |
Company Name | LIVONGO HEALTH, 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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | 800.945.4355 |
membersupport@livongo.com |
Handling Environment Atmospheric Pressure | Between 0 KiloPascal and 75 KiloPascal |
Handling Environment Atmospheric Pressure | Between 0 KiloPascal and 75 KiloPascal |
Handling Environment Atmospheric Pressure | Between 0 KiloPascal and 75 KiloPascal |
Handling Environment Atmospheric Pressure | Between 0 KiloPascal and 75 KiloPascal |
Handling Environment Atmospheric Pressure | Between 0 KiloPascal and 75 KiloPascal |
Handling Environment Atmospheric Pressure | Between 0 KiloPascal and 75 KiloPascal |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00853553005318 [Primary] |
NBW | System, Test, Blood Glucose, Over The Counter |
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 | 2017-03-02 |
00853553005318 | BG300, 1 vial of Livongo Test strips, 1 bag of Livongo Sterile Lancets, 1 box of Livongo Contro |
00853553005271 | Livongo Demo Kit with BG300, 1 vial of Livongo Test strips, 1 bag of Livongo Sterile Lancets, 1 |