Primary Device ID | 00840423500004 |
NIH Device Record Key | 9df9a110-5cd7-44f8-a739-021e44d85608 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VivaGuard Ino Blood Glucose Meter |
Version Model Number | VGM01-373 |
Catalog Number | VGM01-373 |
Company DUNS | 119217208 |
Company Name | ABOUND Diagnostics, 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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840423500004 [Primary] |
GS1 | 00840423500677 [Package] Package: Carton [27 Units] In Commercial Distribution |
NBW | System, Test, Blood Glucose, Over The Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-06-11 |
Device Publish Date | 2025-06-03 |
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