eudamed_udi
Primary ID: 04050598013483
PreventID® Entamoeba histolytica (UDI 04050598013483)
Manufactured by Immundiagnostik AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PreventID® Entamoeba histolytica - Primary ID 04050598013483
Device Regulatory Overview
The PreventID® Entamoeba histolytica (Model/Catalog Number: KSTIEH602GP) is a medical device manufactured by Immundiagnostik AG. This product is indexed under FDA Product Code / Category Classification W0105050201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KSTIEH602GP
- Product Code / EMDN
- W0105050201
- Device Name
- PreventID® Entamoeba histolytica
- Database Sync Date
- 2026-08-09 18:44:39
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® Entamoeba histolytica?
The registered manufacturer of record for PreventID® Entamoeba histolytica is Immundiagnostik AG.
What is the Primary UDI-DI identifier for PreventID® Entamoeba histolytica?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04050598013483.
What classification code is assigned to this device?
This device is registered under product classification code W0105050201.
Similar Classification Devices (W0105050201)
Other Devices by Immundiagnostik AG
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