gudid
Primary ID: TES
Kroger (UDI TES)
Manufactured by KROGER CO., THE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kroger - Primary ID TES
Device Regulatory Overview
The Kroger (Model/Catalog Number: TES) is a medical device manufactured by KROGER CO., THE. This product is indexed under FDA Product Code / Category Classification JEQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TES
- Product Code / EMDN
- JEQ
- Device Name
- PTB SMILE SONIC MAX PWR PRO
- 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 Kroger?
The registered manufacturer of record for Kroger is KROGER CO., THE.
What is the Primary UDI-DI identifier for Kroger?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TES.
What classification code is assigned to this device?
This device is registered under product classification code JEQ.
Similar Classification Devices (JEQ)
Other Devices by KROGER CO., THE
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