| Primary Device ID | 00858724003469 |
| NIH Device Record Key | d47be4ee-38a2-49b7-9ce3-dbb147b8f8d8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ARK™ Ethyl Glucuronide Assay |
| Version Model Number | 5036-0001-00 |
| Catalog Number | 5036-0001-00 |
| Company DUNS | 164880598 |
| Company Name | ARK DIAGNOSTICS 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 | 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 |
| Phone | 5102706270 |
| customersupport@ark-tdm.com |
| Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00858724003469 [Primary] |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-12-25 |
| 00858724003629 | The ARK™ Ethyl Glucuronide Assay is intended for the qualitative and semiquantitative determi |
| 00858724003612 | The ARK™ Ethyl Glucuronide Assay is intended for the qualitative and semiquantitative determi |
| 00858724003605 | The ARK™ Ethyl Glucuronide Assay is intended for the qualitative and semiquantitative determi |
| 00858724003469 | The ARK™ Ethyl Glucuronide Assay is intended for the qualitative and semiquantitative determi |