Human IgG3 Subclass Liquid Reagent Kit for use on

GUDID 05051700006132

THE BINDING SITE GROUP LIMITED

Immunoglobulin G subclass (IgG subclass) IVD, kit, nephelometry/turbidimetry

• Primary Device ID: 05051700006132
• NIH Device Record Key: 9f7c81e1-95e3-4841-ba4d-72ec79f2379d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Human IgG3 Subclass Liquid Reagent Kit for use on
• Version Model Number: LK008.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

Customer Support Contacts

• Phone: +4401214569500
• Email: info@bindingsite.co.uk

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	05051700006132 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090920

FDA Product Code

• CFN: Method, Nephelometric, Immunoglobulins (G, A, M)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-09-14
• Device Publish Date: 2016-09-24

On-Brand Devices [Human IgG3 Subclass Liquid Reagent Kit for use on ]

• 05051700016391: LK008.10S
• 05051700007764: NK008.T
• 05051700006163: LK008.TB
• 05051700006132: LK008.H
• 05051700006101: LK008.2TB