gudid
Primary ID: 82001
Cavitron (UDI 82001)
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 82001
Device Regulatory Overview
The Cavitron (Model/Catalog Number: 82001) 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
- 82001
- Product Code / EMDN
- ELC
- Device Name
- FOCUSED SPRAY PowerLINE FITGRIP Ultrasonic Insert 30K FSI-PWR-3 FG
- Database Sync Date
- 2026-08-09 09:02:02
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 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 82001.
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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