| Primary Device ID | 30014613336686 |
| NIH Device Record Key | e1f368c2-2c4a-42d9-a645-7b2e617499f4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AdenoPlus |
| Version Model Number | RPS-AD |
| Catalog Number | RPS-AD |
| Company DUNS | 079509836 |
| Company Name | QUIDEL CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 30014613336686 [Primary] |
| GOD | ANTIGENS, CF (INCLUDING CF CONTROL), ADENOVIRUS 1-33 |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-12-11 |
| Device Publish Date | 2018-11-10 |
| 30014613336747 - InflammaDry | 2023-06-16 InflammaDry |
| 30014613336754 - InflammaDry | 2023-06-16 InflammaDry |
| 30014613339755 - Sofia 2 | 2023-04-05 Sofia 2 SARS Ag + FIA |
| 30014613202783 - Solana | 2022-06-10 Solana instrument |
| 30014613339670 - QuickVue | 2021-05-14 QuickVue At-Home OTC COVID-19 Test |
| 30014613339687 - QuickVue | 2021-05-10 QuickVue At-Home OTC COVID-19 Test |
| 30014613339724 - QuickVue | 2021-05-10 QuickVue At-Home OTC COVID-19 Test |
| 30014613339083 - Sofia | 2021-02-25 Sofia® SARS Antigen FIA |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ADENOPLUS 85686361 4305076 Dead/Cancelled |
QUIDEL CORPORATION 2012-07-25 |