eudamed_udi
Primary ID: D-MD168UE
Vagiflor (UDI D-MD168UE)
Manufactured by HÄLSA Pharma GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vagiflor - Primary ID D-MD168UE
Device Regulatory Overview
The Vagiflor (Model/Catalog Number: 30010413) is a medical device manufactured by HÄLSA Pharma GmbH. This product is indexed under FDA Product Code / Category Classification U0803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30010413
- Product Code / EMDN
- U0803
- Device Name
- Vagiflor
- Database Sync Date
- 2026-08-09 16:58:30
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 Vagiflor?
The registered manufacturer of record for Vagiflor is HÄLSA Pharma GmbH.
What is the Primary UDI-DI identifier for Vagiflor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-MD168UE.
What classification code is assigned to this device?
This device is registered under product classification code U0803.
Similar Classification Devices (U0803)
Other Devices by HÄLSA Pharma GmbH
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