Boston Aesthetics

GUDID 06971782588014

Shenzhen Peninsula Medical Group Co., Ltd.

Electrosurgical system

• Primary Device ID: 06971782588014
• NIH Device Record Key: 57bf2a63-e220-4165-9260-77246d0a2ca2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Boston Aesthetics
• Version Model Number: Unicorn+ I
• Company DUNS: 544317730
• Company Name: Shenzhen Peninsula Medical Group Co., Ltd.
• 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: false
• Serial Number: true
• Manufacturing Date: true
• 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	06971782588014 [Primary]

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2025-06-23
• Device Publish Date: 2025-06-13

On-Brand Devices [Boston Aesthetics]

• 06971782588038: Unicorn+ III
• 06971782588021: Unicorn+ II
• 06971782588014: Unicorn+ I
• 06971782588007: Unicorn+