COVID-19 Neutralizing Ab Test (UDI 06958982140938)
Manufactured by Abiores Technology (Beijing) Co.,Ltd.
Device Regulatory Overview
The COVID-19 Neutralizing Ab Test (Model/Catalog Number: ACA21B005-001D) is a medical device manufactured by Abiores Technology (Beijing) Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0105040699 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACA21B005-001D
- Product Code / EMDN
- W0105040699
- Device Name
- COVID-19 Neutralizing Ab Test
- Database Sync Date
- 2026-08-09 17:05:13
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 COVID-19 Neutralizing Ab Test?
The registered manufacturer of record for COVID-19 Neutralizing Ab Test is Abiores Technology (Beijing) Co.,Ltd..
What is the Primary UDI-DI identifier for COVID-19 Neutralizing Ab Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958982140938.
What classification code is assigned to this device?
This device is registered under product classification code W0105040699.
Similar Classification Devices (W0105040699)
Other Devices by Abiores Technology (Beijing) Co.,Ltd.
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