eudamed_udi
Primary ID: 04719873130146
Pulmogine® (UDI 04719873130146)
Manufactured by HCmed Innovations Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pulmogine® - Primary ID 04719873130146
Device Regulatory Overview
The Pulmogine® (Model/Catalog Number: DP-P001) is a medical device manufactured by HCmed Innovations Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R9001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DP-P001
- Product Code / EMDN
- R9001
- Device Name
- Mouthpiece
- Database Sync Date
- 2026-08-09 18:42:19
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 Pulmogine®?
The registered manufacturer of record for Pulmogine® is HCmed Innovations Co., Ltd..
What is the Primary UDI-DI identifier for Pulmogine®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719873130146.
What classification code is assigned to this device?
This device is registered under product classification code R9001.
Similar Classification Devices (R9001)
Other Devices by HCmed Innovations Co., Ltd.
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