Trifocus Blue

GUDID 00842894147702

Diversified Products, Inc.

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