Evoke

GUDID 00092006001075

Liquid Personal Lubricant

GUY & O'NEILL, INC.

Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant Sexual lubricant

• Primary Device ID: 00092006001075
• NIH Device Record Key: 80010a8e-9536-493c-8ff2-7dd0c53aa416
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Evoke
• Version Model Number: 900-025
• Company DUNS: 037838844
• Company Name: GUY & O'NEILL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com
• Phone: 262-692-2469
• Email: customerservice@guyandoneill.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00092006001075 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160763

FDA Product Code

• NUC: Lubricant, Personal

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-08-09
• Device Publish Date: 2017-04-19