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 |