10 eyevan

GUDID 04582669019150

EYEVAN INC.

Tinted non-prescription spectacles

• Primary Device ID: 04582669019150
• NIH Device Record Key: 1fac9cd5-eace-4aa9-87b2-39b0c8313fdf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 10 eyevan
• Version Model Number: NO.9 5(48) 48 12S-CL
• Company DUNS: 705184505
• Company Name: EYEVAN 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04582669019150 [Primary]

FDA Product Code

• HQY: Sunglasses (Non-Prescription Including Photosensitive)

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: 2025-01-06
• Device Publish Date: 2024-12-27

On-Brand Devices [10 eyevan]

• 04582669019181: NO.9 5(48) 48 15S-CL
• 04582669019167: NO.9 5(48) 48 13S-CL
• 04582669019150: NO.9 5(48) 48 12S-CL
• 04582669019143: NO.9 5(48) 48 11S-CL
• 04582669019136: NO.9 5(48) 48 4S-CL