Primary Device ID | 05214002307035 |
NIH Device Record Key | 24d4edc9-2481-4abc-a9a2-408e40fdf18a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Advantis Platform |
Version Model Number | 4 |
Company DUNS | 523550273 |
Company Name | ADVANTIS MEDICAL IMAGING SINGLE MEMBER P.C. |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io | |
Phone | +302109329558 |
info@advantis.io |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05214002307035 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-01 |
Device Publish Date | 2024-01-24 |