GUDIDData
gudid Primary ID: 20 tests/kit

Macro & Micro-Test LH Test (UDI 20 tests/kit)

Manufactured by Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Macro & Micro-Test LH Test - Primary ID 20 tests/kit

Device Regulatory Overview

The Macro & Micro-Test LH Test (Model/Catalog Number: 20 tests/kit) is a medical device manufactured by Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NGE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
20 tests/kit
Product Code / EMDN
NGE
Device Name
Database Sync Date
2026-08-09 09:06:37

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 Macro & Micro-Test LH Test?

The registered manufacturer of record for Macro & Micro-Test LH Test is Jiangsu Macro & Micro-Test Med-Tech Co., Ltd..

What is the Primary UDI-DI identifier for Macro & Micro-Test LH Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20 tests/kit.

What classification code is assigned to this device?

This device is registered under product classification code NGE.

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JSON API Endpoint