eudamed_udi
Primary ID: 04251778107323
Refluthin (UDI 04251778107323)
Manufactured by HÄLSA Pharma GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Refluthin - Primary ID 04251778107323
Device Regulatory Overview
The Refluthin (Model/Catalog Number: 573302) is a medical device manufactured by HÄLSA Pharma GmbH. This product is indexed under FDA Product Code / Category Classification G0401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 573302
- Product Code / EMDN
- G0401
- Device Name
- Refluthin
- Database Sync Date
- 2026-08-09 17:02:02
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 Refluthin?
The registered manufacturer of record for Refluthin is HÄLSA Pharma GmbH.
What is the Primary UDI-DI identifier for Refluthin?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251778107323.
What classification code is assigned to this device?
This device is registered under product classification code G0401.
Similar Classification Devices (G0401)
Other Devices by HÄLSA Pharma GmbH
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