gudid
Primary ID: 0021352FG
Pro-Sonic (UDI 0021352FG)
Manufactured by DENTSPLY INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pro-Sonic - Primary ID 0021352FG
Device Regulatory Overview
The Pro-Sonic (Model/Catalog Number: 0021352FG) is a medical device manufactured by DENTSPLY INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification EFT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0021352FG
- Product Code / EMDN
- EFT
- Device Name
- Pro-Sonic Tartar & Stain Remover
- Database Sync Date
- 2026-08-09 09:03:03
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 Pro-Sonic?
The registered manufacturer of record for Pro-Sonic is DENTSPLY INTERNATIONAL INC..
What is the Primary UDI-DI identifier for Pro-Sonic?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0021352FG.
What classification code is assigned to this device?
This device is registered under product classification code EFT.
Similar Classification Devices (EFT)
Other Devices by DENTSPLY INTERNATIONAL INC.
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