GUDIDData
gudid Primary ID: HWTS-AIO800

EudemonTM AIO800 (UDI HWTS-AIO800)

Manufactured by Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EudemonTM AIO800 - Primary ID HWTS-AIO800

Device Regulatory Overview

The EudemonTM AIO800 (Model/Catalog Number: HWTS-AIO800) is a medical device manufactured by Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NSU within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
HWTS-AIO800
Product Code / EMDN
NSU
Device Name
Database Sync Date
2026-08-09 09:06:37

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 EudemonTM AIO800?

The registered manufacturer of record for EudemonTM AIO800 is Jiangsu Macro & Micro-Test Med-Tech Co., Ltd..

What is the Primary UDI-DI identifier for EudemonTM AIO800?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HWTS-AIO800.

What classification code is assigned to this device?

This device is registered under product classification code NSU.

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