| Primary Device ID | 05051700006064 |
| NIH Device Record Key | 7f1bb3b1-bf08-4e02-b3e4-3b78d66f57c6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hu IgG Subclass Liquid Reagent Kits for use on Hit |
| Version Model Number | LK001.H |
| 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 |
| Phone | +4401214569500 |
| info@bindingsite.co.uk |
| Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05051700006064 [Primary] |
| DFZ | Igg (Gamma Chain Specific), Antigen, Antiserum, Control |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-09-14 |
| Device Publish Date | 2016-09-24 |
| 05051700021036 - Optilite® IgG3 Kit (x10) | 2023-10-05 |
| 05051700021043 - Optilite® IgG4 Kit (x10) | 2023-10-05 |
| 05051700016803 - Freelite® Kappa AMR Check Fluid SD | 2023-08-17 |
| 05051700016810 - Freelite® Lambda AMR Check Fluid SD | 2023-08-17 |
| 05051700002059 - Freelite® Panel Sample Set | 2023-07-07 |
| 05051700010696 - Human Alpha 1 Antitrypsin NL BINDARID™ Kit | 2023-07-07 |
| 05051700015974 - IgD AMR Fluid | 2023-06-15 |
| 05051700015981 - B2M AMR Fluid | 2023-06-15 |