eudamed_udi
Primary ID: 04719873130313
Aerogen® Go (UDI 04719873130313)
Manufactured by HCmed Innovations Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aerogen® Go - Primary ID 04719873130313
Device Regulatory Overview
The Aerogen® Go (Model/Catalog Number: DP-M001) is a medical device manufactured by HCmed Innovations Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R03010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DP-M001
- Product Code / EMDN
- R03010301
- Device Name
- Mask (Adult)
- Database Sync Date
- 2026-08-09 17:13:02
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 Aerogen® Go?
The registered manufacturer of record for Aerogen® Go is HCmed Innovations Co., Ltd..
What is the Primary UDI-DI identifier for Aerogen® Go?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719873130313.
What classification code is assigned to this device?
This device is registered under product classification code R03010301.
Similar Classification Devices (R03010301)
Other Devices by HCmed Innovations Co., Ltd.
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