Floravi

GUDID 00688504005402

WESTRIDGE LABORATORIES INCORPORATED

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 Sexual lubricant

• Primary Device ID: 00688504005402
• NIH Device Record Key: 43c09655-4969-4195-af27-da8f2c1b1f46
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Floravi
• Version Model Number: 1 oz Water Based 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	00688504005402 [Primary]

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: 2
• Public Version Date: 2018-08-09
• Device Publish Date: 2018-03-06

On-Brand Devices [Floravi]

• 00688504005402: 1 oz Water Based Disc Cap Bottle
• 30688504003461: This is a water-based personal lubricant and is compatible with both Polyurethane and Latex Cond
• 30688504003454: A silicone lubricant that is latex compatible.