RxLAL Post Op Spectacles

GUDID 00818806020487

Post Op Spectacles

RXSIGHT, INC.

Tinted spectacle lens, non-prescription

• Primary Device ID: 00818806020487
• NIH Device Record Key: c9fe261f-3e19-44ef-8a97-194bc6429a1b
• Commercial Distribution Discontinuation: 2019-05-02
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: RxLAL Post Op Spectacles
• Version Model Number: 62016
• 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: 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	00818806020487 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-05-03
• Device Publish Date: 2019-04-08

On-Brand Devices [RxLAL Post Op Spectacles]

• 00818806020487: Post Op Spectacles
• 00818806020326: Post Op Spectacles
• 00818806020500: Post Op Spectacles, Large
• 00818806020494: Post Op Spectacles