gudid
Primary ID: 130203
Cavitron (UDI 130203)
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 130203
Device Regulatory Overview
The Cavitron (Model/Catalog Number: 130203) is a medical device manufactured by Dentsply Professional. This product is indexed under FDA Product Code / Category Classification KOJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 130203
- Product Code / EMDN
- KOJ
- Device Name
- Cavitron JET-Fresh Mint Flavored Prophy Powder with Aluminimum Trihydroxide 364g
- 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
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 130203.
What classification code is assigned to this device?
This device is registered under product classification code KOJ.
Similar Classification Devices (KOJ)
Other Devices by Dentsply Professional
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint