GUDIDData
eudamed_udi Primary ID: D-697994388Nc032ZLDC

Unspecified Brand (UDI D-697994388Nc032ZLDC)

Manufactured by Kangsheng Information Technology (Hangzhou) Co. LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID D-697994388Nc032ZLDC

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: Nc032) is a medical device manufactured by Kangsheng Information Technology (Hangzhou) Co. LTD. This product is indexed under FDA Product Code / Category Classification W0105041101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Nc032
Product Code / EMDN
W0105041101
Device Name
Human Coronavirus (OC43/229E/HKU1/NL63) Nucleic Acid Detection Kit
Database Sync Date
2026-08-09 16:50:08

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 Kangsheng Information Technology (Hangzhou) 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 D-697994388Nc032ZLDC.

What classification code is assigned to this device?

This device is registered under product classification code W0105041101.

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