gudid
Primary ID: 130314
NUPRO (UDI 130314)
Manufactured by Dentsply Professional
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NUPRO - Primary ID 130314
Device Regulatory Overview
The NUPRO (Model/Catalog Number: 130314) is a medical device manufactured by Dentsply Professional. This product is indexed under FDA Product Code / Category Classification LBH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 130314
- Product Code / EMDN
- LBH
- Device Name
- NUPRO 5% Sodium Fluoride White Varnish, Patient Dose Kit - BubbleGum. Contents: Integrated Brush, 500 Patient Doses of 0.4g.
- 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?
The registered manufacturer of record for NUPRO is Dentsply Professional.
What is the Primary UDI-DI identifier for NUPRO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 130314.
What classification code is assigned to this device?
This device is registered under product classification code LBH.
Similar Classification Devices (LBH)
Other Devices by Dentsply Professional
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