FRITZ EYEWEAR

GUDID 08012794011720

PLASTIC FRAME WITH SUNLENSES

LA GIARDINIERA SRL

Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles

• Primary Device ID: 08012794011720
• NIH Device Record Key: a76779f0-9ae6-40f3-bb12-92d5eadfad79
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FRITZ EYEWEAR
• Version Model Number: PLASTIC SUNGLASSES
• Company DUNS: 428689665
• Company Name: LA GIARDINIERA SRL
• 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	08012794011720 [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: 2023-10-04
• Device Publish Date: 2023-09-26

On-Brand Devices [FRITZ EYEWEAR]

• 08012794011737: SPECTACLE FRAME WITH DEMOLENSES
• 08012794011720: PLASTIC FRAME WITH SUNLENSES