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 |