eudamed_udi Primary ID: 06957469402668

Respiratory Humidifier (UDI 06957469402668)

Manufactured by Shenyang RMS Medical Tech Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Respiratory Humidifier (Model/Catalog Number: HUMID-CM) is a medical device manufactured by Shenyang RMS Medical Tech Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification R060201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: HUMID-CM
Product Code / EMDN: R060201
Device Name: Respiratory Humidifier
Database Sync Date: 2026-08-09 17:20:34

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 Respiratory Humidifier?

The registered manufacturer of record for Respiratory Humidifier is Shenyang RMS Medical Tech Co.,Ltd..

What is the Primary UDI-DI identifier for Respiratory Humidifier?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06957469402668.

What classification code is assigned to this device?

This device is registered under product classification code R060201.

Similar Classification Devices (R060201)

Other Devices by Shenyang RMS Medical Tech Co.,Ltd.

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