| Primary Device ID | D7075820640 |
| NIH Device Record Key | 55c52d29-4de4-44f8-aa74-3ce0d26f0874 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Minigold |
| Version Model Number | 582064 |
| Catalog Number | 582064 |
| Company DUNS | 176935203 |
| Company Name | IVOCLAR VIVADENT, INC. |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D7075820640 [Primary] |
| EJT | Alloy, gold-based noble metal |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-04-27 |
| Device Publish Date | 2018-10-29 |
| D7075766280 | Minigold 25 g |
| D7075820650 | Minigold 100 g |
| D7075820640 | Minigold 1oz/31 g |
| D7075820620 | Minigold 5 g |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MINIGOLD 73017568 1007779 Live/Registered |
WILLIAMS GOLD REFINING COMPANY, INCORPORATED 1974-04-01 |