Primary Device ID | 00851950008147 |
NIH Device Record Key | 122f1f49-123b-4284-a900-c07f2a42a460 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arvolife |
Version Model Number | Drug Test Panel |
Company DUNS | 827033924 |
Company Name | Clinical Guard |
Device Count | 5 |
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 | false |
OTC Over-The-Counter | true |