gudid
Primary ID: 81514
Cavitron (UDI 81514)
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 81514
Device Regulatory Overview
The Cavitron (Model/Catalog Number: 81514) 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
- 81514
- Product Code / EMDN
- ELC
- Device Name
- Bellissima FOCUSED SPRAY slimLINE Ultrasonic Insert 30K (B) FSI-SLI 2-Pack. Contains: one 30K FSI-SLI 10R, one 30K FSI-SLI 10L
- 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 81514.
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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