gudid
Primary ID: 60606596
Capsule Extruder 2 (UDI 60606596)
Manufactured by Dentsply De Trey GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Capsule Extruder 2 - Primary ID 60606596
Device Regulatory Overview
The Capsule Extruder 2 (Model/Catalog Number: 60606596) is a medical device manufactured by Dentsply De Trey GmbH. This product is indexed under FDA Product Code / Category Classification KXR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 60606596
- Product Code / EMDN
- KXR
- Device Name
- Capsule Extruder 2 is the device designed for extrusion and direct application ofChemFil Rock restorative capsules
- 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 Capsule Extruder 2?
The registered manufacturer of record for Capsule Extruder 2 is Dentsply De Trey GmbH.
What is the Primary UDI-DI identifier for Capsule Extruder 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 60606596.
What classification code is assigned to this device?
This device is registered under product classification code KXR.
Similar Classification Devices (KXR)
Other Devices by Dentsply De Trey GmbH
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