GUDIDData
eudamed_udi Primary ID: 06974323012115

Unspecified Brand (UDI 06974323012115)

Manufactured by Beijing Applied Biological Technologies Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06974323012115

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: CT8022-24T) is a medical device manufactured by Beijing Applied Biological Technologies Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0105070399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CT8022-24T
Product Code / EMDN
W0105070399
Device Name
Duplex Real-Time PCR Detection Kit for Coxsackievirus A16 and Human Enterovirus 71
Database Sync Date
2026-08-09 16:30:17

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Beijing Applied Biological Technologies Co., Ltd..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974323012115.

What classification code is assigned to this device?

This device is registered under product classification code W0105070399.

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