gudid
Primary ID: T162020
Neuroglide Back Neck Pad (UDI T162020)
Manufactured by Eva Medtec, Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neuroglide Back Neck Pad - Primary ID T162020
Device Regulatory Overview
The Neuroglide Back Neck Pad (Model/Catalog Number: T162020) is a medical device manufactured by Eva Medtec, Inc. This product is indexed under FDA Product Code / Category Classification IRP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T162020
- Product Code / EMDN
- IRP
- Device Name
- Back/Neck Therapy attachment used in conjunction with the Neuroglide Controller Unit
- Database Sync Date
- 2026-08-09 09:04:02
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 Neuroglide Back Neck Pad?
The registered manufacturer of record for Neuroglide Back Neck Pad is Eva Medtec, Inc.
What is the Primary UDI-DI identifier for Neuroglide Back Neck Pad?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is T162020.
What classification code is assigned to this device?
This device is registered under product classification code IRP.
Similar Classification Devices (IRP)
Other Devices by Eva Medtec, Inc
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