eudamed_udi
Primary ID: 04251778108948
Aspecton Hustenstiller (UDI 04251778108948)
Manufactured by HÄLSA Pharma GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aspecton Hustenstiller - Primary ID 04251778108948
Device Regulatory Overview
The Aspecton Hustenstiller (Model/Catalog Number: 14012) is a medical device manufactured by HÄLSA Pharma GmbH. This product is indexed under FDA Product Code / Category Classification Q030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 14012
- Product Code / EMDN
- Q030199
- Device Name
- Aspecton Hustenstiller
- Database Sync Date
- 2026-08-09 16:50:07
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 Aspecton Hustenstiller?
The registered manufacturer of record for Aspecton Hustenstiller is HÄLSA Pharma GmbH.
What is the Primary UDI-DI identifier for Aspecton Hustenstiller?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251778108948.
What classification code is assigned to this device?
This device is registered under product classification code Q030199.
Similar Classification Devices (Q030199)
Other Devices by HÄLSA Pharma GmbH
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