eudamed_udi Primary ID: 06921963710437

Rapid DOA-7 Panel Test Cup (UDI 06921963710437)

Manufactured by Xiamen Boson Biotech Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Rapid DOA-7 Panel Test Cup (Model/Catalog Number: 1L23K3) 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: 1L23K3
Product Code / EMDN: W0102160511
Device Name: Rapid DOA-7 Panel Test Cup
Database Sync Date: 2026-08-09 16:44:47

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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Frequently Asked Questions

Who is the primary manufacturer of Rapid DOA-7 Panel Test Cup?

The registered manufacturer of record for Rapid DOA-7 Panel Test Cup is Xiamen Boson Biotech Co., Ltd..

What is the Primary UDI-DI identifier for Rapid DOA-7 Panel Test Cup?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06921963710437.

What classification code is assigned to this device?

This device is registered under product classification code W0102160511.

Similar Classification Devices (W0102160511)

Other Devices by Xiamen Boson Biotech Co., Ltd.

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