Nuon (UDI HD-53B)

Manufactured by Shenzhen Nuon Medical Equipment Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Nuon (Model/Catalog Number: HD-53B) is a medical device manufactured by Shenzhen Nuon Medical Equipment Co., Ltd.. This product is indexed under FDA Product Code / Category Classification OLP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: HD-53B
Product Code / EMDN: OLP
Device Name
Database Sync Date: 2026-08-09 09:18:21

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 Nuon?

The registered manufacturer of record for Nuon is Shenzhen Nuon Medical Equipment Co., Ltd..

What is the Primary UDI-DI identifier for Nuon?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HD-53B.

What classification code is assigned to this device?

This device is registered under product classification code OLP.

Similar Classification Devices (OLP)

Other Devices by Shenzhen Nuon Medical Equipment Co., Ltd.

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