gudid
Primary ID: MyndMove FES System
MyndMove 2.0 (UDI MyndMove FES System)
Manufactured by MyndTec Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MyndMove 2.0 - Primary ID MyndMove FES System
Device Regulatory Overview
The MyndMove 2.0 (Model/Catalog Number: MyndMove FES System) is a medical device manufactured by MyndTec Inc. This product is indexed under FDA Product Code / Category Classification IPF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MyndMove FES System
- Product Code / EMDN
- IPF
- Device Name
- Database Sync Date
- 2026-08-09 09:04:20
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 MyndMove 2.0?
The registered manufacturer of record for MyndMove 2.0 is MyndTec Inc.
What is the Primary UDI-DI identifier for MyndMove 2.0?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MyndMove FES System.
What classification code is assigned to this device?
This device is registered under product classification code IPF.
Similar Classification Devices (IPF)
Other Devices by MyndTec Inc
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