Primary Device ID | 90850018992445 |
NIH Device Record Key | cd672e31-31da-46e3-9709-b70f18653842 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | t:connect Mobile Application, Mobile Bolus Enabled (Android) |
Version Model Number | 1007112 |
Company DUNS | 827900809 |
Company Name | TANDEM DIABETES CARE, 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 | 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 | 90850018992445 [Primary] |
PJT | Continuous Glucose Monitor Secondary Display |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-04-25 |
Device Publish Date | 2022-04-15 |
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