Primary Device ID | 00858724003766 |
NIH Device Record Key | be8f8bc3-23cf-4c01-93d4-91a62157200e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ARK™ Ethyl Glucuronide Control (750/1250) |
Version Model Number | 5036-0006-01 |
Catalog Number | 5036-0006-01 |
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 |