gudid
Primary ID: S12
Stimulation System (UDI S12)
Manufactured by Edan Instruments, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Stimulation System - Primary ID S12
Device Regulatory Overview
The Stimulation System (Model/Catalog Number: S12) is a medical device manufactured by Edan Instruments, Inc.. This product is indexed under FDA Product Code / Category Classification IPF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S12
- Product Code / EMDN
- IPF
- Device Name
- Database Sync Date
- 2026-08-09 09:11:05
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 Stimulation System?
The registered manufacturer of record for Stimulation System is Edan Instruments, Inc..
What is the Primary UDI-DI identifier for Stimulation System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S12.
What classification code is assigned to this device?
This device is registered under product classification code IPF.
Similar Classification Devices (IPF)
Other Devices by Edan Instruments, Inc.
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