BURT

GUDID 00867504000406

BARRETT TECHNOLOGY, LLC

Virtual-display rehabilitation system, powered-support

• Primary Device ID: 00867504000406
• NIH Device Record Key: 318ad505-1e4f-441b-bdf2-ab7f19700425
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BURT
• Version Model Number: M1200
• Company DUNS: 080108367
• Company Name: BARRETT TECHNOLOGY, LLC
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00867504000406 [Primary]

FDA Product Code

• IKK: System, Isokinetic Testing And Evaluation

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-20
• Device Publish Date: 2017-11-14

On-Brand Devices [BURT]

• 00867504000413: BURT Rehabilitation System is indicated to aid in the rehabilitation and evaluation of upper ext
• 00867504000406: M1200