gudid
Primary ID: 8800004
Cavitron (UDI 8800004)
Manufactured by Dentsply Professional
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cavitron - Primary ID 8800004
Device Regulatory Overview
The Cavitron (Model/Catalog Number: 8800004) is a medical device manufactured by Dentsply Professional. This product is indexed under FDA Product Code / Category Classification ELC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8800004
- Product Code / EMDN
- ELC
- Device Name
- Cavitron integrated systems Built-In Ultrasonic Scaler Model G139 Dealer Kit (82 SURF, S/M 360) Also contains: Handpiece with swivel cable, Ultrasonic insert, Installation kit and Power Supply.
- Database Sync Date
- 2026-08-09 09:02:02
Full Regulatory Attributes
🔒 Token Gated
{
"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 Cavitron?
The registered manufacturer of record for Cavitron is Dentsply Professional.
What is the Primary UDI-DI identifier for Cavitron?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8800004.
What classification code is assigned to this device?
This device is registered under product classification code ELC.
Similar Classification Devices (ELC)
Other Devices by Dentsply Professional
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