Smartlite Pro Endo Activator Activator (UDI 644435)
Manufactured by Dentsply International Inc.
Device Regulatory Overview
The Smartlite Pro Endo Activator Activator (Model/Catalog Number: 644435) is a medical device manufactured by Dentsply International Inc.. This product is indexed under FDA Product Code / Category Classification EKQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 644435
- Product Code / EMDN
- EKQ
- Device Name
- Database Sync Date
- 2026-08-09 09:02:03
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 Smartlite Pro Endo Activator Activator?
The registered manufacturer of record for Smartlite Pro Endo Activator Activator is Dentsply International Inc..
What is the Primary UDI-DI identifier for Smartlite Pro Endo Activator Activator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 644435.
What classification code is assigned to this device?
This device is registered under product classification code EKQ.
Similar Classification Devices (EKQ)
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