Primary Device ID | 10190302018135 |
NIH Device Record Key | e8b27e46-afcb-45a6-8d9c-ee9b070b6794 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Diomni™ Software, V3.1.0 |
Version Model Number | A54762 |
Company DUNS | 080131636 |
Company Name | LIFE TECHNOLOGIES CORPORATION |
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 |
---|---|
GS1 | 10190302018135 [Primary] |
OOI | real time Nucleic acid amplification system |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-20 |
Device Publish Date | 2022-09-12 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DIOMNI 90788551 not registered Live/Pending |
Life Technologies Corporation 2021-06-22 |