ID Xtreme

GUDID 00761236107054

WESTRIDGE LABORATORIES INCORPORATED

Sexual lubricant

• Primary Device ID: 00761236107054
• NIH Device Record Key: ee670f30-9384-423f-a99e-6147a09c1a42
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ID Xtreme
• Version Model Number: ID Xtreme 2.2 fl oz Disc Cap Bottle
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00761236107054 [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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-08-09
• Device Publish Date: 2018-03-06

On-Brand Devices [ID Xtreme]

• 00761236107085: ID Xtreme 3 ml Foils
• 30761236107079: ID Xtreme 8.5 fl oz Disc Cap Bottle
• 00761236107061: ID Xtreme 4.4 fl oz Disc Cap Bottle
• 00761236107054: ID Xtreme 2.2 fl oz Disc Cap Bottle
• 40761236107045: ID Xtreme 1 fl oz Pocket Bottle