Primary Device ID | B35000300R0 |
NIH Device Record Key | 606961bb-2fce-4397-942a-3436b3d823b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ThunderBolt EIA |
Version Model Number | 00300R |
Catalog Number | 00300R |
Company DUNS | 790524891 |
Company Name | Gold Standard Diagnostics Corporation |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |