GUDIDData
eudamed_udi Primary ID: 04251934201759

Unspecified Brand (UDI 04251934201759)

Manufactured by Shenzhen Keborui Electronics Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 04251934201759

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: NA) is a medical device manufactured by Shenzhen Keborui Electronics Co., Ltd. This product is indexed under FDA Product Code / Category Classification K02010203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NA
Product Code / EMDN
K02010203
Device Name
Connection Cable
Database Sync Date
2026-08-09 16:28:52

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 Shenzhen Keborui Electronics 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 04251934201759.

What classification code is assigned to this device?

This device is registered under product classification code K02010203.

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