gudid
Primary ID: MyndMove Electrode 3cm x 1cm
MyndMove (UDI MyndMove Electrode 3cm x 1cm)
Manufactured by MyndTec Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MyndMove - Primary ID MyndMove Electrode 3cm x 1cm
Device Regulatory Overview
The MyndMove (Model/Catalog Number: MyndMove Electrode 3cm x 1cm) 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 Electrode 3cm x 1cm
- 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?
The registered manufacturer of record for MyndMove is MyndTec Inc.
What is the Primary UDI-DI identifier for MyndMove?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MyndMove Electrode 3cm x 1cm.
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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