gudid Primary ID: None

2-Microglobin Kit (Latex-Enhanced Immunoturbidimetric Method) (UDI None)

Manufactured by Medicalsystem Biotechnology Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The 2-Microglobin Kit (Latex-Enhanced Immunoturbidimetric Method) (Model/Catalog Number: None) is a medical device manufactured by Medicalsystem Biotechnology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification JZG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: None
Product Code / EMDN: JZG
Device Name
Database Sync Date: 2026-08-09 09:06:49

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 2-Microglobin Kit (Latex-Enhanced Immunoturbidimetric Method)?

The registered manufacturer of record for 2-Microglobin Kit (Latex-Enhanced Immunoturbidimetric Method) is Medicalsystem Biotechnology Co., Ltd..

What is the Primary UDI-DI identifier for 2-Microglobin Kit (Latex-Enhanced Immunoturbidimetric Method)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is None.

What classification code is assigned to this device?

This device is registered under product classification code JZG.

Similar Classification Devices (JZG)

Other Devices by Medicalsystem Biotechnology Co., Ltd.

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