Primary Device ID | 00853341006053 |
NIH Device Record Key | 70b23440-2da5-4e0d-ba7c-c28fc355d3de |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HeartFlow Analysis |
Version Model Number | FFRct version 3 |
Company DUNS | 804411283 |
Company Name | HEARTFLOW, 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 | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |