Compressor Nebulizer (UDI 06947832500213)
Manufactured by Shenzhen Aeon Technology Co., Ltd.
Device Regulatory Overview
The Compressor Nebulizer (Model/Catalog Number: A500LWD04) is a medical device manufactured by Shenzhen Aeon Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12159002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A500LWD04
- Product Code / EMDN
- Z12159002
- Device Name
- Compressor Nebulizer
- Database Sync Date
- 2026-08-09 17:09:54
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 Compressor Nebulizer?
The registered manufacturer of record for Compressor Nebulizer is Shenzhen Aeon Technology Co., Ltd..
What is the Primary UDI-DI identifier for Compressor Nebulizer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06947832500213.
What classification code is assigned to this device?
This device is registered under product classification code Z12159002.
Similar Classification Devices (Z12159002)
Other Devices by Shenzhen Aeon Technology Co., Ltd.
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