Fidelity

GUDID 06977267470041

A&E Fashion Group Co., Ltd.

Tinted non-prescription spectacles

• Primary Device ID: 06977267470041
• NIH Device Record Key: a2d1a1ca-123d-4561-b151-97b57059c429
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fidelity
• Version Model Number: (01)06977267470041(10)202404(11)20240401
• Company DUNS: 540162528
• Company Name: A&E Fashion Group Co., 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: true
• Serial Number: true
• Manufacturing Date: true
• 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	06977267470041 [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: 2024-06-19
• Device Publish Date: 2024-06-11

Devices Manufactured by A&E Fashion Group Co., Ltd.

• 06977267470003 - Jagger: 2024-06-19
• 06977267470010 - NUTRL: 2024-06-19
• 06977267470027 - NUTRL: 2024-06-19
• 06977267470034 - NUTRL: 2024-06-19
• 06977267470041 - Fidelity: 2024-06-19
• 06977267470041 - Fidelity: 2024-06-19