Portable Mesh Nebulizer kit (UDI 06973912940433)
Manufactured by Shenzhen IMDK Medical Technology Co.,Ltd.
Device Regulatory Overview
The Portable Mesh Nebulizer kit (Model/Catalog Number: YM-3RB) is a medical device manufactured by Shenzhen IMDK Medical Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification R03010304 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- YM-3RB
- Product Code / EMDN
- R03010304
- Device Name
- Portable Mesh Nebulizer kit
- Database Sync Date
- 2026-08-09 16:30:01
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Portable Mesh Nebulizer kit?
The registered manufacturer of record for Portable Mesh Nebulizer kit is Shenzhen IMDK Medical Technology Co.,Ltd..
What is the Primary UDI-DI identifier for Portable Mesh Nebulizer kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973912940433.
What classification code is assigned to this device?
This device is registered under product classification code R03010304.
Similar Classification Devices (R03010304)
Other Devices by Shenzhen IMDK Medical Technology Co.,Ltd.
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