BRIUS

GUDID 00860002991009

Brius Technologies Inc

Orthodontic wire

• Primary Device ID: 00860002991009
• NIH Device Record Key: 032a53c8-e2fc-4992-9653-10690a42d588
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BRIUS
• Version Model Number: 1
• Company DUNS: 117587817
• Company Name: Brius Technologies Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860002991009 [Primary]

FDA Product Code

• DZC: Wire, Orthodontic

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: 2020-10-30
• Device Publish Date: 2020-10-22

Devices Manufactured by Brius Technologies Inc

• 00860002991016 - BRIUS Clear Aligner: 2023-03-14 BRIUS Clear Aligner
• 00860002991009 - BRIUS: 2020-10-30
• 00860002991009 - BRIUS: 2020-10-30