Rapid DOA-5 Panel Test (UDI 06921963710383)
Manufactured by Xiamen Boson Biotech Co., Ltd.
Device Regulatory Overview
The Rapid DOA-5 Panel Test (Model/Catalog Number: 1L21M3) is a medical device manufactured by Xiamen Boson Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160511 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1L21M3
- Product Code / EMDN
- W0102160511
- Device Name
- Rapid DOA-5 Panel Test
- Database Sync Date
- 2026-08-09 16:30:08
Full Regulatory Attributes
๐ Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Rapid DOA-5 Panel Test?
The registered manufacturer of record for Rapid DOA-5 Panel Test is Xiamen Boson Biotech Co., Ltd..
What is the Primary UDI-DI identifier for Rapid DOA-5 Panel Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06921963710383.
What classification code is assigned to this device?
This device is registered under product classification code W0102160511.
Similar Classification Devices (W0102160511)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint