TheraMist

GUDID B1870800

Electrolyte solution, 4 oz. spray bottle

NEUROTRON MEDICAL, INC.

Electrode conductive medium

• Primary Device ID: B1870800
• NIH Device Record Key: 645eb4da-4ba4-407e-aa7d-7e85aee134f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TheraMist
• Version Model Number: TKA-0216
• Company DUNS: 147018519
• Company Name: NEUROTRON MEDICAL, 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: true
• Serial Number: false
• Manufacturing Date: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B1870800 [Primary]

FDA Product Code

• GYB: Media, Electroconductive

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: 2024-12-12
• Device Publish Date: 2024-12-04

On-Brand Devices [TheraMist]

• B1870180: Electrolyte solution, 8 oz. spray bottle
• B1870800: Electrolyte solution, 4 oz. spray bottle