Braun Silk Expert 5

GUDID 00069055886199

Light Based Over-The-Counter Hair Removal

PROCTER & GAMBLE MANUFACTURING COMPANY, THE

Cosmetic red-light phototherapy system, home-use

• Primary Device ID: 00069055886199
• NIH Device Record Key: 4b4a0898-0da4-4001-bd57-a92bc6de9a44
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Braun Silk Expert 5
• Version Model Number: BD5004
• Company DUNS: 004238200
• Company Name: PROCTER & GAMBLE MANUFACTURING COMPANY, THE
• 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: true
• 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

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00069055886199 [Primary]
GS1	10069055886196 [Package]; Package: box [2 Units]; 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: 2
• Public Version Date: 2020-02-24
• Device Publish Date: 2018-12-21

On-Brand Devices [Braun Silk Expert 5]

• 00069055886199: Light Based Over-The-Counter Hair Removal
• 10069055880958: Light Based Over-The-Counter Hair Removal