RapidFor™ Entamoeba histolytica Test Kit (UDI 08685115800589)
Manufactured by Vitrosens Biotechnology Inc.
Device Regulatory Overview
The RapidFor™ Entamoeba histolytica Test Kit (Model/Catalog Number: VMD100 ) is a medical device manufactured by Vitrosens Biotechnology Inc.. This product is indexed under FDA Product Code / Category Classification W0105050201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VMD100
- Product Code / EMDN
- W0105050201
- Device Name
- Entamoeba histolytica Test Kit
- Database Sync Date
- 2026-08-09 17:33:12
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 RapidFor™ Entamoeba histolytica Test Kit ?
The registered manufacturer of record for RapidFor™ Entamoeba histolytica Test Kit is Vitrosens Biotechnology Inc..
What is the Primary UDI-DI identifier for RapidFor™ Entamoeba histolytica Test Kit ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08685115800589.
What classification code is assigned to this device?
This device is registered under product classification code W0105050201.
Similar Classification Devices (W0105050201)
Other Devices by Vitrosens Biotechnology Inc.
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