GUDIDData
gudid Primary ID: 2MHz

NA (UDI 2MHz)

Manufactured by Edan Instruments, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID 2MHz

Device Regulatory Overview

The NA (Model/Catalog Number: 2MHz) is a medical device manufactured by Edan Instruments, Inc.. This product is indexed under FDA Product Code / Category Classification KNG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2MHz
Product Code / EMDN
KNG
Device Name
Database Sync Date
2026-08-09 09:11:06

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 NA?

The registered manufacturer of record for NA is Edan Instruments, Inc..

What is the Primary UDI-DI identifier for NA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2MHz.

What classification code is assigned to this device?

This device is registered under product classification code KNG.

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