GUDIDData
eudamed_udi Primary ID: 06972820961233

ST4307 (UDI 06972820961233)

Manufactured by Shenzhen SINO-K Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ST4307 - Primary ID 06972820961233

Device Regulatory Overview

The ST4307 (Model/Catalog Number: 07-10-00) is a medical device manufactured by Shenzhen SINO-K Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification V03010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
07-10-00
Product Code / EMDN
V03010201
Device Name
Temperature Probe
Database Sync Date
2026-08-09 18:41:28

Full Regulatory Attributes

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{
    "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 ST4307?

The registered manufacturer of record for ST4307 is Shenzhen SINO-K Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for ST4307?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972820961233.

What classification code is assigned to this device?

This device is registered under product classification code V03010201.

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