GUDIDData
eudamed_udi Primary ID: 06970952640002

Unspecified Brand (UDI 06970952640002)

Manufactured by Jiangsu Kehua Medical Instrument Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06970952640002

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: N/A) is a medical device manufactured by Jiangsu Kehua Medical Instrument Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W050302010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
N/A
Product Code / EMDN
W050302010102
Device Name
Plastic pipette(Plastic dropper/Plastic capillary tube)
Database Sync Date
2026-08-09 16:30:31

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 Jiangsu Kehua Medical Instrument Technology 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 06970952640002.

What classification code is assigned to this device?

This device is registered under product classification code W050302010102.

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