eudamed_udi Primary ID: 06921963710314

Rapid Oxycodone Test Card (UDI 06921963710314)

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 Oxycodone Test Card (Model/Catalog Number: 1L16C3) is a medical device manufactured by Xiamen Boson Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1L16C3
Product Code / EMDN: W0102160599
Device Name: Rapid Oxycodone Test Card
Database Sync Date: 2026-08-09 16:28:57

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 Oxycodone Test Card?

The registered manufacturer of record for Rapid Oxycodone Test Card is Xiamen Boson Biotech Co., Ltd..

What is the Primary UDI-DI identifier for Rapid Oxycodone Test Card?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06921963710314.

What classification code is assigned to this device?

This device is registered under product classification code W0102160599.

Similar Classification Devices (W0102160599)

Other Devices by Xiamen Boson Biotech Co., Ltd.

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