eudamed_udi
Primary ID: 06970389634056
Electrical stimulator (UDI 06970389634056)
Manufactured by Famidoc Technology Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Electrical stimulator - Primary ID 06970389634056
Device Regulatory Overview
The Electrical stimulator (Model/Catalog Number: FDES105) is a medical device manufactured by Famidoc Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification N010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FDES105
- Product Code / EMDN
- N010103
- Device Name
- Electrical stimulator
- Database Sync Date
- 2026-08-09 18:08:35
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 Electrical stimulator?
The registered manufacturer of record for Electrical stimulator is Famidoc Technology Co., Ltd..
What is the Primary UDI-DI identifier for Electrical stimulator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970389634056.
What classification code is assigned to this device?
This device is registered under product classification code N010103.
Similar Classification Devices (N010103)
Other Devices by Famidoc Technology Co., Ltd.
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