eudamed_udi
Primary ID: 04050598013353
PreventID® H. pylori (UDI 04050598013353)
Manufactured by Immundiagnostik AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PreventID® H. pylori - Primary ID 04050598013353
Device Regulatory Overview
The PreventID® H. pylori (Model/Catalog Number: KST18116GP) is a medical device manufactured by Immundiagnostik AG. This product is indexed under FDA Product Code / Category Classification W0105010402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KST18116GP
- Product Code / EMDN
- W0105010402
- Device Name
- PreventID® H. pylori
- Database Sync Date
- 2026-08-09 16:44:50
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 PreventID® H. pylori?
The registered manufacturer of record for PreventID® H. pylori is Immundiagnostik AG.
What is the Primary UDI-DI identifier for PreventID® H. pylori?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04050598013353.
What classification code is assigned to this device?
This device is registered under product classification code W0105010402.
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Other Devices by Immundiagnostik AG
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