Primary Device ID | 00856596006168 |
NIH Device Record Key | 0506ad34-e912-431e-b0d8-7a76ab72a06a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CariFree |
Version Model Number | Mint |
Company DUNS | 195544965 |
Company Name | Dental Alliance Holdings LLC |
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 | false |
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 | 00856596006168 [Primary] |
LBH | Varnish, Cavity |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-02-23 |
Device Publish Date | 2023-02-15 |
00856596006168 | A mixture of 5% sodium fluoride in a resin carrier, packaged in a convenient single-use dose for |
00856596006151 | A mixture of 5% sodium fluoride in a resin carrier, packaged in a convenient single-use dose for |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CARIFREE 98442388 not registered Live/Pending |
DENTAL ALLIANCE HOLDINGS, LLC DBA ORAL BIOTECH 2024-03-10 |
CARIFREE 85810165 4438892 Live/Registered |
DENTAL ALLIANCE HOLDINGS, LLC DBA ORAL BIOTECH 2012-12-24 |
CARIFREE 85810164 4438891 Live/Registered |
DENTAL ALLIANCE HOLDINGS, LLC DBA ORAL BIOTECH 2012-12-24 |
CARIFREE 85810161 4438890 Live/Registered |
DENTAL ALLIANCE HOLDINGS, LLC DBA ORAL BIOTECH 2012-12-24 |
CARIFREE 78604181 3137190 Dead/Cancelled |
Bowers, Robert J 2005-04-07 |