eudamed_udi
Primary ID: 06944413811935
Biofeedback and Stimulation System (UDI 06944413811935)
Manufactured by Edan Instruments,Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Biofeedback and Stimulation System - Primary ID 06944413811935
Device Regulatory Overview
The Biofeedback and Stimulation System (Model/Catalog Number: P2) is a medical device manufactured by Edan Instruments,Inc.. This product is indexed under FDA Product Code / Category Classification U070399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P2
- Product Code / EMDN
- U070399
- Device Name
- Biofeedback and Stimulation System
- Database Sync Date
- 2026-08-09 16:45:53
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 Biofeedback and Stimulation System?
The registered manufacturer of record for Biofeedback and Stimulation System is Edan Instruments,Inc..
What is the Primary UDI-DI identifier for Biofeedback and Stimulation System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06944413811935.
What classification code is assigned to this device?
This device is registered under product classification code U070399.
Similar Classification Devices (U070399)
Other Devices by Edan Instruments,Inc.
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