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 |