SKELETON

GUDID 08012794011508

PAIR OF SPARE SUNLENSES

LA GIARDINIERA SRL

Tinted non-prescription spectacle lens

• Primary Device ID: 08012794011508
• NIH Device Record Key: bc4312c7-b334-4ab6-89fe-d07f7cf49a6a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SKELETON
• Version Model Number: PLASTIC SUNLENSES
• 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	08012794011508 [Primary]

FDA Product Code

• HQG: Lens, Spectacle, Non-Custom (Prescription)

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: 2023-05-04
• Device Publish Date: 2023-04-26

On-Brand Devices [SKELETON]

• 08012794011508: PAIR OF SPARE SUNLENSES
• 08012794011492: PLASTIC FRAME WITH SUNLENSES