Primary Device ID | 00817713020023 |
NIH Device Record Key | b82f3d60-48f9-4e5a-9d11-1373fb3d70c8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ORAPRO |
Version Model Number | J104K |
Company DUNS | 192699952 |
Company Name | ORTHOQUEST, 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 | true |
Device Combination Product | false |
Single Use | false |
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 | 00817713020023 [Primary] |
DYH | Adhesive, Bracket And Tooth Conditioner, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-20 |
00817713022997 | ORAPRO G2 LC BAND CEMENT BLUE KIT 6/5GM |
00817713022959 | ORAPRO G2 LC ADHESIVE KIT 4/5GM SYRINGE |
00817713022942 | ORAPRO G2 LC ADHESIVE INTRO KIT 1/5GM SYRINGE |
00817713020146 | ORTHQST ETCH 4-12G BLUE W/TIPS (UNLAB) |
00817713020139 | ORTHQST EC CERT ORAPRO LC ADH INTRO KIT |
00817713020047 | ORTHQST ORAPRO LC BAND CEM BLUE 1-5G KIT |
00817713020030 | ORTHQST ORAPRO NO MIX ADH INTRO KIT |
00817713020023 | ORTHQST ORAPRO LC 4-3.5G ADH KIT |
00817713020016 | ORTHQST ORAPRO LC ADH INTRO KIT |
10817713022970 | ORAPRO G2 7ML LC BONDING RESIN |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ORAPRO 76979236 4305438 Live/Registered |
ORTHOQUEST, INC. 2011-11-07 |
ORAPRO 76709660 4481306 Live/Registered |
Health Care Suppliers, Inc. 2011-11-07 |
ORAPRO 76509724 3038889 Live/Registered |
ORTHOQUEST, INC. 2003-04-28 |