Optilite Caeruloplasmin Kit

GUDID 05051700018197

THE BINDING SITE GROUP LIMITED

Ceruloplasmin IVD, kit, nephelometry/turbidimetry
Primary Device ID05051700018197
NIH Device Record Key6fcfc254-cb28-4e6f-8c89-2e89798e4baf
Commercial Distribution StatusIn Commercial Distribution
Brand NameOptilite Caeruloplasmin Kit
Version Model NumberNK045.OPT.A
Company DUNS347045614
Company NameTHE BINDING SITE GROUP LIMITED
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4401214569500
Emailinfo@bindingsite.co.uk

Operating and Storage Conditions

Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS105051700018197 [Primary]

FDA Product Code

DDBCeruloplasmin, Antigen, Antiserum, Control

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-24

Devices Manufactured by THE BINDING SITE GROUP LIMITED

05051700019392 - Optilite® Low Level Total Protein Controls2024-11-07
05051700020534 - Optilite® Low Level Total Protein Calibrator2024-11-07
05051700020558 - Optilite® Low Level Total Protein Reagent2024-11-07
05051700021036 - Optilite® IgG3 Kit (x10)2023-10-05
05051700021043 - Optilite® IgG4 Kit (x10)2023-10-05
05051700016803 - Freelite® Kappa AMR Check Fluid SD2023-08-17
05051700016810 - Freelite® Lambda AMR Check Fluid SD2023-08-17
05051700002059 - Freelite® Panel Sample Set2023-07-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.