bt-sculpt GEN2

GUDID 00817076014523

bt-sculpt GEN2 - Stainless Steel

MICRO CURRENT TECHNOLOGY, INC.

Analgesic transcutaneous electrical nerve stimulation system

• Primary Device ID: 00817076014523
• NIH Device Record Key: ea786227-b6bb-4b50-8bf2-5c06b0f82b7c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: bt-sculpt GEN2
• Version Model Number: MF-88
• Company DUNS: 121167779
• Company Name: MICRO CURRENT TECHNOLOGY, INC.
• 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817076014523 [Primary]

FDA Product Code

• NFO: Stimulator, Transcutaneous Electrical, Aesthetic Purposes

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: 2025-08-14
• Device Publish Date: 2025-08-06

On-Brand Devices [bt-sculpt GEN2]

• 00817076014530: bt-sculpt GEN2 - Blue
• 00817076014523: bt-sculpt GEN2 - Stainless Steel
• 00817076014516: bt-sculpt GEN2 - White