gudid
Primary ID: 8161427
Cavitron (UDI 8161427)
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 8161427
Device Regulatory Overview
The Cavitron (Model/Catalog Number: 8161427) 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
- 8161427
- Product Code / EMDN
- ELC
- Device Name
- Cavitron prophy-jet Package. Also contains: Cavitron Prophy-Jet Air Polishing System, JET-Mate Sterilizable Detachable Handpieces, JET Air Polishing Inserts, Prophy-JET Sodium Bicarbonate Powder 13 Oz. Bottle, JET-Fresh Aluminum Trihydroxide Prophy Powder 13 Oz. Bottle, Cavitron Care Maintenance Plan Registration Information.
- 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 8161427.
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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