Primary Device ID | 05051700006118 |
NIH Device Record Key | f4e5ed0b-e152-42a1-a211-17c991387e60 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Olympus IgG3 Kit |
Version Model Number | LK008.AU |
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 | 05051700006118 [Primary] |
CFN | Method, Nephelometric, Immunoglobulins (G, A, M) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-24 |
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