GUDIDData
gudid Primary ID: NS40300

NETWORK (UDI NS40300)

Manufactured by NETWORK MEDICAL PRODUCTS LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NETWORK - Primary ID NS40300

Device Regulatory Overview

The NETWORK (Model/Catalog Number: NS40300) is a medical device manufactured by NETWORK MEDICAL PRODUCTS LIMITED. This product is indexed under FDA Product Code / Category Classification HOZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NS40300
Product Code / EMDN
HOZ
Device Name
NS40300 PVA Spears Non-sterile 5 Piece
Database Sync Date
2026-08-09 09:08:11

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 NETWORK?

The registered manufacturer of record for NETWORK is NETWORK MEDICAL PRODUCTS LIMITED.

What is the Primary UDI-DI identifier for NETWORK?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NS40300.

What classification code is assigned to this device?

This device is registered under product classification code HOZ.

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