| Primary Device ID | 00816594021600 |
| NIH Device Record Key | a9f6f7f7-778d-4d0c-9ee9-c333f3780aaa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MICROPRIME |
| Version Model Number | 87001 |
| Catalog Number | 87001 |
| Company DUNS | 601302743 |
| Company Name | DANVILLE MATERIALS, LLC |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| 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(760)743-7744 |
| xxx@xxx.xxx | |
| Phone | +1(760)743-7744 |
| xxx@xxx.xxx | |
| Phone | +1(760)743-7744 |
| xxx@xxx.xxx |
| Storage Environment Temperature | Between 0 and 74 Degrees Fahrenheit |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816594021600 [Primary] |
| KLE | AGENT, TOOTH BONDING, RESIN |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2016-06-22 |
| 00816594021617 | MICROPRIME G,UD,50 |
| 00816594021600 | MICROPRIME B,10ML,FA |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MICROPRIME 98532431 not registered Live/Pending |
Zest IP Holdings, LLC 2024-05-03 |
![]() MICROPRIME 88384865 not registered Live/Pending |
Andes Ag, Inc. 2019-04-14 |
![]() MICROPRIME 86489770 not registered Dead/Abandoned |
Professional Disposables International,Inc. 2014-12-23 |