NUPRO Prophylaxis Paste with Fluoride (UDI 80312)
Manufactured by DENTSPLY INTERNATIONAL INC.
Device Regulatory Overview
The NUPRO Prophylaxis Paste with Fluoride (Model/Catalog Number: 80312) is a medical device manufactured by DENTSPLY INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification EJR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 80312
- Product Code / EMDN
- EJR
- Device Name
- NUPRO Prophy Paste, Zinnamon, Coarse, Single Box (200 cups)
- 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 NUPRO Prophylaxis Paste with Fluoride?
The registered manufacturer of record for NUPRO Prophylaxis Paste with Fluoride is DENTSPLY INTERNATIONAL INC..
What is the Primary UDI-DI identifier for NUPRO Prophylaxis Paste with Fluoride?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 80312.
What classification code is assigned to this device?
This device is registered under product classification code EJR.
Similar Classification Devices (EJR)
Other Devices by DENTSPLY INTERNATIONAL INC.
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