Primary Device ID | 05051700018319 |
NIH Device Record Key | ff57eef5-d6dc-47ee-8290-9741dfb944bd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rheumatoid Factor (RF) Kit for use on SPAPLUS |
Version Model Number | LK151.S.A |
Company DUNS | 347045614 |
Company Name | THE BINDING SITE GROUP LIMITED |
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 | false |
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 |