gudid
Primary ID: ET-8080
iReliev (UDI ET-8080)
Manufactured by EXCELHEALTH, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for iReliev - Primary ID ET-8080
Device Regulatory Overview
The iReliev (Model/Catalog Number: ET-8080) is a medical device manufactured by EXCELHEALTH, INC.. This product is indexed under FDA Product Code / Category Classification NYN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ET-8080
- Product Code / EMDN
- NYN
- Device Name
- iReliev iRenew Pain Relief and Recovery System
- Database Sync Date
- 2026-08-09 09:49:31
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 iReliev?
The registered manufacturer of record for iReliev is EXCELHEALTH, INC..
What is the Primary UDI-DI identifier for iReliev?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ET-8080.
What classification code is assigned to this device?
This device is registered under product classification code NYN.
Similar Classification Devices (NYN)
Other Devices by EXCELHEALTH, INC.
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