PRO-TECH

GUDID 00851640007221

SMART-TECH

Hi-Dow International Incorporated

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 00851640007221
• NIH Device Record Key: c2efaf32-4f1c-4dfb-975d-f0ea2fc6eb0b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRO-TECH
• Version Model Number: JQ-5C-E
• Company DUNS: 124034476
• Company Name: Hi-Dow International Incorporated
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851640007221 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102598

FDA Product Code

• NGX: Stimulator, Muscle, Powered, For Muscle Conditioning

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-10-28
• Device Publish Date: 2016-09-01

On-Brand Devices [PRO-TECH]

• 00851640007405: Pro-Tech Wireless
• 00851640007238: MICRO-TECH
• 00851640007221: SMART-TECH
• 00851640007214: PRO-TECH Massager