Primary Device ID | 05051700017541 |
NIH Device Record Key | e8a8e6cb-206d-431e-869d-32b1573ddf33 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Optilite IgG3 |
Version Model Number | LK008.OPT.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 |