LULU

GUDID 00764724769833

Tura Inc.

Spectacle frame

• Primary Device ID: 00764724769833
• NIH Device Record Key: 4401f6ca-f808-49fc-93ad-ef7e457c228b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LULU
• Version Model Number: L163 BLK 53
• Company DUNS: 968237318
• Company Name: Tura 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 18003458872
• Email: kaccts@tura.com

Device Dimensions

• Width: 53 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00764724769833 [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: 2022-10-10
• Device Publish Date: 2022-09-30

On-Brand Devices [LULU]

• 00764724860318: L184 RED 55
• 00764724860301: L184 SLA 55
• 00764724769840: L163 GLD 53
• 00764724769833: L163 BLK 53
• 00764724422233: L155 GLD 54
• 00764724372750: L137 BLK 54
• 00764724296872: L111 BLK 59
• 00764724850319: L181 SLA 53
• 00764724850302: L181 TOR 53
• 00764724848477: L178 IVO 56
• 00764724848460: L178 AMB 56
• 00764724848453: L177 RGD 57
• 00764724848446: L177 GLD 57