Primary Device ID | 09359621000021 |
NIH Device Record Key | 01bcd551-71a4-45c5-b3b5-b2ccab31a1da |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BlueCheck |
Version Model Number | BN01AUS |
Company DUNS | 747210755 |
Company Name | INCISIVE TECHNOLOGIES PTY LTD |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 09359621000021 [Primary] |
LFC | Device, Caries Detection |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-06 |
Device Publish Date | 2025-02-26 |
09359621000014 | BlueCheck Caries Detection & Monitoring Medical Device Dental 0.3 mL x 10 |
09359621000021 | BlueCheck Caries Detection & Monitoring Medical Device Dental 0.3 mL x 1 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BLUECHECK 98131466 not registered Live/Pending |
BlueCheck Charitable Foundation, Inc. 2023-08-14 |
![]() BLUECHECK 79318676 not registered Live/Pending |
INCISIVE TECHNOLOGIES PTY LTD 2021-07-27 |
![]() BLUECHECK 78959070 3260899 Live/Registered |
GEMALTO COGENT, INC. 2006-08-23 |