Choice

GUDID 20860418002614

Blood Glucose Monitoring System, Choice

ARCADIA GROUP

Glucose monitoring system IVD, home-use

• Primary Device ID: 20860418002614
• NIH Device Record Key: e30e2f58-4559-4130-b752-4711ef9a8434
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Choice
• Version Model Number: 8000-10635
• Company DUNS: 555630941
• Company Name: ARCADIA GROUP
• 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• 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: true

Customer Support Contacts

• Phone: 1-800-880-3034
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860418002610 [Primary]
GS1	20860418002614 [Package]; Contains: 00860418002610; Package: Shipper [12 Units]; In Commercial Distribution

FDA Product Code

• NBW: System, Test, Blood Glucose, Over The Counter

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: 2018-10-08
• Device Publish Date: 2018-09-07

On-Brand Devices [Choice]

• 20860418002614: Blood Glucose Monitoring System, Choice
• 20860418002607: Blood Glucose Monitoring System, Choice Basic