Maxim Ignite IDD11123

GUDID 00840281300082

MX24003 Maxim Ignite Personal Lubricant 4.4 fl oz Personal Lubricant

WESTRIDGE LABORATORIES INCORPORATED

Sexual lubricant

• Primary Device ID: 00840281300082
• NIH Device Record Key: 9c973eb2-f07c-4709-871e-4e4eb9243ffe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Maxim Ignite
• Version Model Number: 24003-211019
• Catalog Number: IDD11123
• Company DUNS: 879057065
• Company Name: WESTRIDGE LABORATORIES INCORPORATED
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840281300082 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K051295

FDA Product Code

• NUC: Lubricant, Personal

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: 2021-11-01
• Device Publish Date: 2021-10-22

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