MyRx Visual Acuity

GUDID 07290018993408

6 OVER 6 VISION LTD

Visual acuity projector

• Primary Device ID: 07290018993408
• NIH Device Record Key: ee485092-6c12-4543-ae16-d0c791100dbb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MyRx Visual Acuity
• Version Model Number: 1
• Company DUNS: 600351745
• Company Name: 6 OVER 6 VISION LTD
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290018993408 [Primary]

FDA Product Code

• HOX: Chart, Visual Acuity
• QTO: Digital Visual Acuity Test

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-10-17
• Device Publish Date: 2023-08-30

On-Brand Devices [MyRx Visual Acuity ]

• 72900189934080: 1
• 07290018993408: 1