Braun Silk Expert Pro 5

GUDID 00690558863594

Light Based Over-The-Counter Hair Removal

PROCTER & GAMBLE MANUFACTURING COMPANY, THE

Cosmetic red-light phototherapy system, home-use

• Primary Device ID: 00690558863594
• NIH Device Record Key: 17744429-f15c-4865-a168-bf3e762e721d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Braun Silk Expert Pro 5
• Version Model Number: PL5137
• 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	00690558863594 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2020-01-01

On-Brand Devices [Braun Silk Expert Pro 5]

• 00690558863594: Light Based Over-The-Counter Hair Removal
• 00069055886359: Light Based Over-The-Counter Hair Removal
• 10069055890070: Light Based Over-The-Counter Hair Removal