gudid
Primary ID: FDES108A
Famidoc (UDI FDES108A)
Manufactured by Famidoc Technology Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Famidoc - Primary ID FDES108A
Device Regulatory Overview
The Famidoc (Model/Catalog Number: FDES108A) is a medical device manufactured by Famidoc Technology 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
- FDES108A
- Product Code / EMDN
- IPF
- Device Name
- The stimulator may be used for the following:Symptomatic relief of chronic intractable painPost traumatic painpost surgical painRelaxation of muscle spasm Increase blood flow circulationPrevention or retardation of disuse atrophy Muscle re-education Maintaining or increasing range of motion.Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis.
- Database Sync Date
- 2026-08-09 09:06:49
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 Famidoc?
The registered manufacturer of record for Famidoc is Famidoc Technology Co.,Ltd..
What is the Primary UDI-DI identifier for Famidoc?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FDES108A.
What classification code is assigned to this device?
This device is registered under product classification code IPF.
Similar Classification Devices (IPF)
Other Devices by Famidoc Technology Co.,Ltd.
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