LAMB

GUDID 00764724862558

Tura Inc.

Spectacle frame

• Primary Device ID: 00764724862558
• NIH Device Record Key: 54170e9f-24b2-4fbf-a5d7-a6388178fa5e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LAMB
• Version Model Number: LA586 BLK 56
• 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: 56 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00764724862558 [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 [LAMB]

• 00764724862565: LA586 BLS 56
• 00764724862558: LA586 BLK 56
• 00764724862541: LA585 BLS 57
• 00764724862534: LA585 GLD 57
• 00764724862497: LA583 BLK 59
• 00764724862480: LA583 PUR 59
• 00764724862473: LA582 SLA 54
• 00764724862466: LA582 MUL 54
• 00764724338688: LA509 BLK 55
• 00764724849702: LA577 GLD 61
• 00764724849696: LA577 RGD 61
• 00764724849689: LA580 BON 55
• 00764724849603: LA579 BLK 55
• 00764724849597: LA579 TOR 55
• 00764724849528: LA576 RED 50
• 00764724849511: LA576 YEL 50
• 00764724849504: LA576 TOR 50