gudid
Primary ID: S3
Bodi-Tek (UDI S3)
Manufactured by Shenzhen Leading Perfectin Technology Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bodi-Tek - Primary ID S3
Device Regulatory Overview
The Bodi-Tek (Model/Catalog Number: S3) is a medical device manufactured by Shenzhen Leading Perfectin Technology Co.,Ltd. This product is indexed under FDA Product Code / Category Classification NGX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S3
- Product Code / EMDN
- NGX
- Device Name
- Wireless Electronic Pulse Stimulator for Feet
- Database Sync Date
- 2026-08-09 09:06:39
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 Bodi-Tek?
The registered manufacturer of record for Bodi-Tek is Shenzhen Leading Perfectin Technology Co.,Ltd.
What is the Primary UDI-DI identifier for Bodi-Tek?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S3.
What classification code is assigned to this device?
This device is registered under product classification code NGX.
Similar Classification Devices (NGX)
Other Devices by Shenzhen Leading Perfectin Technology Co.,Ltd
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