Gillette Venus Silk Expert

GUDID 10069055876579

Light Based Over-The-Counter Hair Removal

PROCTER & GAMBLE MANUFACTURING COMPANY, THE

Cosmetic red-light phototherapy system, home-use

• Primary Device ID: 10069055876579
• NIH Device Record Key: 0bdb3901-1cd1-4fe2-a527-177bbaa93169
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Gillette Venus Silk Expert
• Version Model Number: BD5008
• Company DUNS: 004238200
• Company Name: PROCTER & GAMBLE MANUFACTURING COMPANY, THE
• Device Count: 1
• DM Exempt: true
• 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: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)272-8611
• Email: xxx@xxx.xxx

Operating and Storage Conditions

• Storage Environment Temperature: Between -25 Degrees Celsius and 70 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00069055876572 [Primary]
GS1	10069055876579 [Package]; Contains: 00069055876572; Package: Box [2 Units]; Discontinued: 2019-01-31; Not in Commercial Distribution

FDA Product Code

• OHT: Light based over-the-counter hair removal

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-24
• Device Publish Date: 2017-02-01

On-Brand Devices [Gillette Venus Silk Expert]

• 10069055879648: Light Based Over-The-Counter Hair Removal
• 10069055879068: Light Based Over-The-Counter Hair Removal
• 10069055876586: Light Based Over-The-Counter Hair Removal
• 10069055876579: Light Based Over-The-Counter Hair Removal