AdenoPlus RPS-AD
GUDID 30014613336686
AdenoPlus
QUIDEL CORPORATION
Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, immunochromatographic test (ICT), rapid Adenovirus antigen IVD, kit, rapid ICT, clinical Adenovirus antigen IVD, kit, rapid ICT, clinical Adenovirus antigen IVD, kit, rapid ICT, clinical Adenovirus antigen IVD, kit, rapid ICT, clinical Adenovirus antigen IVD, kit, rapid ICT, clinical Adenovirus antigen IVD, kit, rapid ICT, clinical| 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 |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 30014613336686 [Primary] |
FDA Product Code
| GOD | ANTIGENS, CF (INCLUDING CF CONTROL), ADENOVIRUS 1-33 |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-12-11 |
| Device Publish Date | 2018-11-10 |
Devices Manufactured by QUIDEL CORPORATION
| 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 |
Trademark Results [AdenoPlus]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ADENOPLUS 85686361 4305076 Dead/Cancelled |
QUIDEL CORPORATION 2012-07-25 |
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