eudamed_udi
Primary ID: 86060313275786
Entamoeba histolytica (UDI 86060313275786)
Manufactured by NEOMEDICA DOO NIŠ
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Entamoeba histolytica - Primary ID 86060313275786
Device Regulatory Overview
The Entamoeba histolytica (Model/Catalog Number: C1805V24EH) is a medical device manufactured by NEOMEDICA DOO NIŠ. This product is indexed under FDA Product Code / Category Classification W0105050201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C1805V24EH
- Product Code / EMDN
- W0105050201
- Device Name
- Entamoeba histolytica
- Database Sync Date
- 2026-08-09 17:48:32
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 Entamoeba histolytica?
The registered manufacturer of record for Entamoeba histolytica is NEOMEDICA DOO NIŠ.
What is the Primary UDI-DI identifier for Entamoeba histolytica?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 86060313275786.
What classification code is assigned to this device?
This device is registered under product classification code W0105050201.
Similar Classification Devices (W0105050201)
Other Devices by NEOMEDICA DOO NIŠ
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