GUDIDData
gudid Primary ID: 801608

NUPRO Extra Care Prophy Paste with NovaMin (UDI 801608)

Manufactured by DENTSPLY INTERNATIONAL INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NUPRO Extra Care Prophy Paste with NovaMin - Primary ID 801608

Device Regulatory Overview

The NUPRO Extra Care Prophy Paste with NovaMin (Model/Catalog Number: 801608) 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
801608
Product Code / EMDN
EJR
Device Name
NUPRO Extra Care Prophy Paste, Spearmint, Polish w/o Fluoride, 175 Cups
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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Frequently Asked Questions

Who is the primary manufacturer of NUPRO Extra Care Prophy Paste with NovaMin?

The registered manufacturer of record for NUPRO Extra Care Prophy Paste with NovaMin is DENTSPLY INTERNATIONAL INC..

What is the Primary UDI-DI identifier for NUPRO Extra Care Prophy Paste with NovaMin?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 801608.

What classification code is assigned to this device?

This device is registered under product classification code EJR.

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