Ultra+

GUDID 06970441320125

Beijing Anchorfree Technology Co., Ltd.

Hand-held electric massager

• Primary Device ID: 06970441320125
• NIH Device Record Key: a7a7579b-f195-4b99-abb2-06d132cca5d8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ultra+
• Version Model Number: Ultra+
• Company DUNS: 529187417
• Company Name: Beijing Anchorfree Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970441320125 [Primary]

FDA Product Code

• ISA: Massager, Therapeutic, Electric

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: 2025-08-28
• Device Publish Date: 2025-08-20

Devices Manufactured by Beijing Anchorfree Technology Co., Ltd.

• 06970441320132 - AquafirmeXS: 2025-10-01
• 06970441320125 - Ultra+: 2025-08-28
• 06970441320125 - Ultra+: 2025-08-28
• 06970441320019 - Anchorfree: 2020-02-06 The diode laser system is a surgical device intended for use in dermatologic and general surgical procedure. It utilizes a semic