Primary Device ID | 00385930011020 |
NIH Device Record Key | 8c821061-0d99-4714-9737-9813d6ec005a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ultra TRAK PRO Blood Glucose Monitoring System |
Version Model Number | TD-4255 |
Company DUNS | 808107788 |
Company Name | VERTEX DIAGNOSTICS LLC |
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 | false |
Serial Number | true |
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 | 00385930011020 [Primary] |
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 | 2020-01-31 |
Device Publish Date | 2020-01-23 |
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