GUDIDData
gudid Primary ID: None

Total Protein Kit (Biuret Method) (2-Part Reagents) (UDI None)

Manufactured by Medicalsystem Biotechnology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Total Protein Kit (Biuret Method) (2-Part Reagents) - Primary ID None

Device Regulatory Overview

The Total Protein Kit (Biuret Method) (2-Part Reagents) (Model/Catalog Number: None) is a medical device manufactured by Medicalsystem Biotechnology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification CEK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

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

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 Total Protein Kit (Biuret Method) (2-Part Reagents)?

The registered manufacturer of record for Total Protein Kit (Biuret Method) (2-Part Reagents) is Medicalsystem Biotechnology Co., Ltd..

What is the Primary UDI-DI identifier for Total Protein Kit (Biuret Method) (2-Part Reagents)?

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 CEK.

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