Primary Device ID | B236CATL202320 |
NIH Device Record Key | 0bdc985f-e9c7-411d-9925-3c0c5b3e3468 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Clinisys Atlas |
Version Model Number | 2023.2 |
Company DUNS | 052934841 |
Company Name | CliniSys, Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B236CATL202320 [Primary] |
JQP | Calculator/Data Processing Module, For Clinical Use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-11 |
Device Publish Date | 2023-12-01 |
B236ATL2023100 | Clinisys Atlas is a solution set comprised of four solutions that can be activated individually |
B236CATL202320 | Clinisys Atlas is a solution set comprised of four solutions that can be activated individually |
B236CATL202330 | Clinisys Atlas is a solution set comprised of four solutions that can be activated individually |
B236CATL202340 | Clinisys Atlas is a solution set comprised of four solutions that can be activated individually |