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 |