GUDIDData
gudid Primary ID: NRF0404

Neoendo Retreatment File (UDI NRF0404)

Manufactured by ORIKAM HEALTHCARE INDIA PRIVATE LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neoendo Retreatment File - Primary ID NRF0404

Device Regulatory Overview

The Neoendo Retreatment File (Model/Catalog Number: NRF0404) is a medical device manufactured by ORIKAM HEALTHCARE INDIA PRIVATE LIMITED. This product is indexed under FDA Product Code / Category Classification EKS within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NRF0404
Product Code / EMDN
EKS
Device Name
Dental Rotary File
Database Sync Date
2026-08-09 09:01:55

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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Frequently Asked Questions

Who is the primary manufacturer of Neoendo Retreatment File?

The registered manufacturer of record for Neoendo Retreatment File is ORIKAM HEALTHCARE INDIA PRIVATE LIMITED.

What is the Primary UDI-DI identifier for Neoendo Retreatment File?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NRF0404.

What classification code is assigned to this device?

This device is registered under product classification code EKS.

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