gudid
Primary ID: 60013954
Dentronix (UDI 60013954)
Manufactured by DENTRONIX INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dentronix - Primary ID 60013954
Device Regulatory Overview
The Dentronix (Model/Catalog Number: 60013954) is a medical device manufactured by DENTRONIX INC. This product is indexed under FDA Product Code / Category Classification EBZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 60013954
- Product Code / EMDN
- EBZ
- Device Name
- LED 3000 Charger Base
- Database Sync Date
- 2026-08-09 09:03:07
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 Dentronix?
The registered manufacturer of record for Dentronix is DENTRONIX INC.
What is the Primary UDI-DI identifier for Dentronix?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 60013954.
What classification code is assigned to this device?
This device is registered under product classification code EBZ.
Similar Classification Devices (EBZ)
Other Devices by DENTRONIX INC
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