gudid
Primary ID: TENS 7
Liberty (UDI TENS 7)
Manufactured by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Liberty - Primary ID TENS 7
Device Regulatory Overview
The Liberty (Model/Catalog Number: TENS 7) is a medical device manufactured by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.. This product is indexed under FDA Product Code / Category Classification IPF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TENS 7
- Product Code / EMDN
- IPF
- Device Name
- Electrical Muscel Stimulator (EMS)
- Database Sync Date
- 2026-08-09 09:15:29
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Liberty?
The registered manufacturer of record for Liberty is EVERYWAY MEDICAL INSTRUMENTS CO., LTD..
What is the Primary UDI-DI identifier for Liberty?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TENS 7.
What classification code is assigned to this device?
This device is registered under product classification code IPF.
Similar Classification Devices (IPF)
Other Devices by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
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