gudid
Primary ID: SmartRelief 1.0 - Back/Hip Kit
Icy Hot SmartRelief (UDI SmartRelief 1.0 - Back/Hip Kit)
Manufactured by CHATTEM, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Icy Hot SmartRelief - Primary ID SmartRelief 1.0 - Back/Hip Kit
Device Regulatory Overview
The Icy Hot SmartRelief (Model/Catalog Number: SmartRelief 1.0 - Back/Hip Kit) is a medical device manufactured by CHATTEM, INC.. This product is indexed under FDA Product Code / Category Classification NYN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SmartRelief 1.0 - Back/Hip Kit
- Product Code / EMDN
- NYN
- Device Name
- Over-The-Counter (OTC) Transcutaneous Electrical Nerve Stimulator (TENS) - Back & Hip
- Database Sync Date
- 2026-08-09 09:08:52
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 Icy Hot SmartRelief?
The registered manufacturer of record for Icy Hot SmartRelief is CHATTEM, INC..
What is the Primary UDI-DI identifier for Icy Hot SmartRelief?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SmartRelief 1.0 - Back/Hip Kit.
What classification code is assigned to this device?
This device is registered under product classification code NYN.
Similar Classification Devices (NYN)
Other Devices by CHATTEM, INC.
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