eudamed_udi Primary ID: 06973912940457

Portable Mesh Nebulizer (UDI 06973912940457)

Manufactured by Shenzhen IMDK Medical Technology Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Portable Mesh Nebulizer (Model/Catalog Number: YM-3R7) is a medical device manufactured by Shenzhen IMDK Medical Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification R03010302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: YM-3R7
Product Code / EMDN: R03010302
Device Name: Portable Mesh Nebulizer
Database Sync Date: 2026-08-09 18:06:15

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 Portable Mesh Nebulizer?

The registered manufacturer of record for Portable Mesh Nebulizer is Shenzhen IMDK Medical Technology Co.,Ltd..

What is the Primary UDI-DI identifier for Portable Mesh Nebulizer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973912940457.

What classification code is assigned to this device?

This device is registered under product classification code R03010302.

Similar Classification Devices (R03010302)

Other Devices by Shenzhen IMDK Medical Technology Co.,Ltd.

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