Welllead Mesh Nebulizer Kit (UDI 06925816646461)
Manufactured by Well Lead Medical Co., Ltd.
Device Regulatory Overview
The Welllead Mesh Nebulizer Kit (Model/Catalog Number: R01L023020) is a medical device manufactured by Well Lead Medical 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
- R01L023020
- Product Code / EMDN
- R03010304
- Device Name
- Mesh Nebulizer Kit
- Database Sync Date
- 2026-08-09 16:29:38
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 Welllead Mesh Nebulizer Kit?
The registered manufacturer of record for Welllead Mesh Nebulizer Kit is Well Lead Medical Co., Ltd..
What is the Primary UDI-DI identifier for Welllead Mesh Nebulizer Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06925816646461.
What classification code is assigned to this device?
This device is registered under product classification code R03010304.
Similar Classification Devices (R03010304)
Other Devices by Well Lead Medical Co., Ltd.
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