E-Fit

GUDID 05999887598012

Fit-Pro Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 05999887598012
• NIH Device Record Key: 6c974796-7698-4487-89af-4d426de36f7b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E-Fit
• Version Model Number: EF-1280
• Company DUNS: 366811421
• Company Name: Fit-Pro Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05999887598012 [Primary]

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: 4
• Public Version Date: 2019-10-23
• Device Publish Date: 2017-02-16

On-Brand Devices [E-Fit]

• 05999887598012: EF-1280
• 05999887598029: Infinity