Primary Device ID | 00348783004793 |
NIH Device Record Key | 0197cc75-44fe-4dfc-b124-46d4fbd8feed |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cure-Thru Clear Cervical Matrices |
Version Model Number | 9061013 |
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 | 00348783004793 [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 |