RapidFor™ AFP Rapid Test Kit (FIA) (UDI 08683548250896)
Manufactured by Vitrosens Biotechnology Inc.
Device Regulatory Overview
The RapidFor™ AFP Rapid Test Kit (FIA) (Model/Catalog Number: VMPO51) is a medical device manufactured by Vitrosens Biotechnology Inc.. This product is indexed under FDA Product Code / Category Classification W0102039001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VMPO51
- Product Code / EMDN
- W0102039001
- Device Name
- AFP Rapid Test Kit (FIA)
- Database Sync Date
- 2026-08-09 17:28:17
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™ AFP Rapid Test Kit (FIA)?
The registered manufacturer of record for RapidFor™ AFP Rapid Test Kit (FIA) is Vitrosens Biotechnology Inc..
What is the Primary UDI-DI identifier for RapidFor™ AFP Rapid Test Kit (FIA)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683548250896.
What classification code is assigned to this device?
This device is registered under product classification code W0102039001.
Similar Classification Devices (W0102039001)
Other Devices by Vitrosens Biotechnology Inc.
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