Trifocus Blue

GUDID 00842894147702

Diversified Products, Inc.

Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles Magnifying spectacles

• Primary Device ID: 00842894147702
• NIH Device Record Key: 6986d6a0-87d0-4e2d-adb7-63e2c0c53bdc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trifocus Blue
• Version Model Number: BX2201-125
• Company DUNS: 604170506
• Company Name: Diversified Products, 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: false
• Lot Batch: false
• Serial Number: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842894147702 [Primary]

FDA Product Code

• HOI: Spectacle, Magnifying

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: 2022-12-13
• Device Publish Date: 2022-12-05

On-Brand Devices [Trifocus Blue]

• 00842894147726: BX2201-175
• 00842894147719: BX2201-150
• 00842894147702: BX2201-125