Primary Device ID | 10850042559021 |
NIH Device Record Key | 7717c84a-f288-4094-8167-9c3efec58ad7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ACCU NEWS Multi-Drug Screen Test |
Version Model Number | Multi-panel |
Company DUNS | 036440919 |
Company Name | CORETESTS, INC. |
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 | false |
Device Combination Product | false |
Single Use | true |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850042559024 [Primary] |
GS1 | 10850042559021 [Package] Contains: 00850042559024 Package: [5 Units] In Commercial Distribution |
DIO | Enzyme Immunoassay, Cocaine And Cocaine Metabolites |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-08 |
Device Publish Date | 2022-08-31 |
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00850042559529 - CorDx Tyfast | 2024-06-21 CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test OTC |
10850042559533 - CorDx Tyfast | 2024-06-21 CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test OTC |
10850042559557 - CorDx Tyfast | 2024-06-21 CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test OTC |
10850042559564 - CorDx Tyfast | 2024-06-21 CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test OTC |
00850042559635 - CorDx Tyfast | 2024-04-19 CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test POC |
10850042559656 - CorDx Tyfast | 2024-04-19 CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test POC |