GUDIDData
eudamed_udi Primary ID: 06975424221819

Anti-SSB Assay Kit (Fluorescence Immunoassay) (UDI 06975424221819)

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 Anti-SSB Assay Kit (Fluorescence Immunoassay) - Primary ID 06975424221819

Device Regulatory Overview

The Anti-SSB Assay Kit (Fluorescence Immunoassay) (Model/Catalog Number: 20T) is a medical device manufactured by DiYaLab ZJG Biotech Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0102100113 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
20T
Product Code / EMDN
W0102100113
Device Name
Anti-SSB Assay Kit (Fluorescence Immunoassay)
Database Sync Date
2026-08-09 16:29:32

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 Anti-SSB Assay Kit (Fluorescence Immunoassay)?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975424221819.

What classification code is assigned to this device?

This device is registered under product classification code W0102100113.

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