GUDIDData
gudid Primary ID: artemis pro

NINGBO YOUHUAN AUTOMATION TECHNOLOGY CO., LTD. (UDI artemis pro)

Manufactured by Ningbo Youhuan Automation Technology Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NINGBO YOUHUAN AUTOMATION TECHNOLOGY CO., LTD. - Primary ID artemis pro

Device Regulatory Overview

The NINGBO YOUHUAN AUTOMATION TECHNOLOGY CO., LTD. (Model/Catalog Number: artemis pro) is a medical device manufactured by Ningbo Youhuan Automation Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification ITI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
artemis pro
Product Code / EMDN
ITI
Device Name
Database Sync Date
2026-08-09 09:06:36

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 NINGBO YOUHUAN AUTOMATION TECHNOLOGY CO., LTD.?

The registered manufacturer of record for NINGBO YOUHUAN AUTOMATION TECHNOLOGY CO., LTD. is Ningbo Youhuan Automation Technology Co., Ltd.

What is the Primary UDI-DI identifier for NINGBO YOUHUAN AUTOMATION TECHNOLOGY CO., LTD.?

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

What classification code is assigned to this device?

This device is registered under product classification code ITI.

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