| Primary Device ID | D813S305500 |
| NIH Device Record Key | f6c425c8-9db8-4d06-991a-2f7b29680c61 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pro-Select3 |
| Version Model Number | S30550 |
| Catalog Number | S30550 |
| Company DUNS | 809857704 |
| Company Name | DEN-MAT 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Phone | 1-800-433-6628 |
| info@denmat.com | |
| Phone | 1-800-433-6628 |
| info@denmat.com |
| Special Storage Condition, Specify | Between 0 and 0 *Do not use this product in presence of inflammable anesthetics or gases |
| Special Storage Condition, Specify | Between 0 and 0 *Do not use this product in presence of inflammable anesthetics or gases |
| Special Storage Condition, Specify | Between 0 and 0 *Do not use this product in presence of inflammable anesthetics or gases |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from explosive substances and flammable materials |
| Special Storage Condition, Specify | Between 0 and 0 *Do not use this product in presence of inflammable anesthetics or gases |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D813S305500 [Primary] |
| ELC | Scaler, Ultrasonic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[D813S305500]
Liquid Chemical;Moist Heat or Steam Sterilization;High-level Disinfectant
[D813S305500]
Liquid Chemical;Moist Heat or Steam Sterilization;High-level Disinfectant
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| D813S307010 | PS3 Foot Pedal |
| D813S305500 | PS3 6ft Autoclave Cable |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PRO-SELECT3 75201696 2155740 Dead/Cancelled |
PROFESSIONAL DENTAL TECHNOLOGIES, INC. 1996-11-21 |