BioCheck Beta-2 Microglobulin EIA Test Kit BC-1061

GUDID 00850392007619

The BioCheck Beta-2 Microglobulin EIA Test Kit is intended for the quantitative determination of beta-2 microglobulin concentration in human serum.

BIOCHECK, INC.

Beta-2-microglobulin IVD, kit, enzyme immunoassay (EIA)

• Primary Device ID: 00850392007619
• NIH Device Record Key: 57fafaee-879e-4f61-896a-b92c66ac29d5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BioCheck Beta-2 Microglobulin EIA Test Kit
• Version Model Number: BC-1061
• Catalog Number: BC-1061
• Company DUNS: 171857493
• Company Name: BIOCHECK, INC.
• 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: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: (650)573-1968
• Email: info@biocheckinc.com
• Phone: (650)573-1968
• Email: info@biocheckinc.com

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850392007619 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K001022

FDA Product Code

• JZG: System, Test, Beta-2-Microglobulin Immunological

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-10-16
• Device Publish Date: 2019-10-08

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