Floravi

GUDID 00688504005402

WESTRIDGE LABORATORIES INCORPORATED

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.