GUDIDData
eudamed_udi Primary ID: 06975424225398

Interleukin - 6 Assay Kit (Fluorescence Immunoassay) (UDI 06975424225398)

Manufactured by DiYaLab ZJG Biotech Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Interleukin - 6 Assay Kit (Fluorescence Immunoassay) - Primary ID 06975424225398

Device Regulatory Overview

The Interleukin - 6 Assay Kit (Fluorescence Immunoassay) (Model/Catalog Number: DL190401C) is a medical device manufactured by DiYaLab ZJG Biotech Co., Ltd. This product is indexed under FDA Product Code / Category Classification W01029099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DL190401C
Product Code / EMDN
W01029099
Device Name
Interleukin - 6 Assay Kit (Fluorescence Immunoassay)
Database Sync Date
2026-08-09 16:50:18

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 Interleukin - 6 Assay Kit (Fluorescence Immunoassay)?

The registered manufacturer of record for Interleukin - 6 Assay Kit (Fluorescence Immunoassay) is DiYaLab ZJG Biotech Co., Ltd.

What is the Primary UDI-DI identifier for Interleukin - 6 Assay Kit (Fluorescence Immunoassay)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975424225398.

What classification code is assigned to this device?

This device is registered under product classification code W01029099.

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