| Primary Device ID | 00348783004779 |
| NIH Device Record Key | 74afe5ea-fb0f-435a-8be7-0cd39447f519 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cure-Thru Clear Cervical Matrices |
| Version Model Number | 9061011 |
| Company DUNS | 014789663 |
| Company Name | PREMIER DENTAL PRODUCTS COMPANY |
| 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 | 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 | 00348783004779 [Primary] |
| JEP | Retainer, Matrix |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-08-14 |
| Device Publish Date | 2024-08-06 |
| 00348783004946 | Positioning Instrument; double-ended, autoclavable |
| 00348783004847 | CURE-THRU CMF BOX 150 - UNIV/MOLAR |
| 00348783004830 | CURE-THRU CMF BOX 150 - ANT/PRE |
| 00348783004823 | CURE-THRU CMF BOX OF 150 723 CT |
| 00348783004816 | CURE-THRU CMF BOX OF 150 722 CT |
| 00348783004809 | CURE-THRU CMF BOX OF 150 721 CT |
| 00348783004793 | CURE-THRU CMF BOX OF 150 720 CT |
| 00348783004786 | CURE-THRU CMF BOX OF 150 719 CT |
| 00348783004779 | CURE-THRU CMF BOX OF 275 ASST |