Womanizer

GUDID 04251460630375

WOW Tech Europe GmbH

Sexual lubricant

• Primary Device ID: 04251460630375
• NIH Device Record Key: a839b0c4-9d60-41bf-8272-378330f76c0b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Womanizer
• Version Model Number: WZ902ALZ
• Company DUNS: 341458344
• Company Name: WOW Tech Europe GmbH
• 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	04251460630375 [Primary]

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: 2024-04-15
• Device Publish Date: 2024-04-05