Post Op Spectacle Readers, Lightweight, +2.5

GUDID 90818806020527

Post Op Spectacle Readers, Lightweight, +2.5

RXSIGHT, INC.

Tinted spectacle lens, non-prescription

• Primary Device ID: 90818806020527
• NIH Device Record Key: af55d0a6-24fe-489c-9351-591fa60610ac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Post Op Spectacle Readers, Lightweight, +2.5
• Version Model Number: 62025-002
• Company DUNS: 052054413
• Company Name: RXSIGHT, 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: true
• Serial Number: false
• 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	90818806020527 [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: 2020-10-08
• Device Publish Date: 2020-09-30

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• 00818806020869 - Light Adjustable Lens (LAL): 2024-12-12 LAL+, Light Adjustable Lens, Sterile, Packaged, 2.0 Diopter
• 00818806020951 - Light Adjustable Lens (LAL): 2024-12-12 LAL+, Light Adjustable Lens, Sterile, Packaged, 1.0 Diopter
• 00818806021484 - Light Adjustable Lens (LAL): 2024-12-12 LAL+, Light Adjustable Lens, Sterile, Packaged, 0.0 Diopter
• 00818806021736 - Light Adjustable Lens (LAL): 2024-12-12 LAL+, Light Adjustable Lens, Sterile, Packaged, -1.0 Diopter