Primary Device ID | 05051700020190 |
NIH Device Record Key | 4ee4273b-9100-4ee7-958c-58ea6ffc1336 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Optilite IgA CSF Kit |
Version Model Number | LK010.L.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 | false |
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 |
Phone | +4401214569500 |
info@bindingsite.co.uk |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05051700020190 [Primary] |
CFN | Method, Nephelometric, Immunoglobulins (G, A, M) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-01 |
Device Publish Date | 2019-06-21 |
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05051700015974 - IgD AMR Fluid | 2023-06-15 |
05051700015981 - B2M AMR Fluid | 2023-06-15 |