Primary Device ID | 08800046800006 |
NIH Device Record Key | 62a27bde-b4a0-45ec-b298-0339f2b53dfe |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ClariCT.AI |
Version Model Number | 1.1.0 |
Company DUNS | 693744312 |
Company Name | ClariPI 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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800046800006 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-12-04 |
Device Publish Date | 2019-12-20 |
08800046800136 | ClariCT.AI, is a software device intended for networking, communication, processing and enhancem |
08800046800006 | 1.1.0 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CLARICT.AI 88550926 not registered Live/Pending |
ClariPI Inc. 2019-07-30 |