GUDIDData
eudamed_udi Primary ID: 06958982140372

CHIK IgG/IgM Test (UDI 06958982140372)

Manufactured by Abiores Technology (Beijing) Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHIK IgG/IgM Test - Primary ID 06958982140372

Device Regulatory Overview

The CHIK IgG/IgM Test (Model/Catalog Number: AB210-20) is a medical device manufactured by Abiores Technology (Beijing) Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0105040699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AB210-20
Product Code / EMDN
W0105040699
Device Name
CHIK IgG/IgM Test
Database Sync Date
2026-08-09 16:50:16

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 CHIK IgG/IgM Test?

The registered manufacturer of record for CHIK IgG/IgM Test is Abiores Technology (Beijing) Co.,Ltd..

What is the Primary UDI-DI identifier for CHIK IgG/IgM Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958982140372.

What classification code is assigned to this device?

This device is registered under product classification code W0105040699.

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