eudamed_udi Primary ID: 06939663977746

One Step Phencyclidine Rapid Test (Urine) (UDI 06939663977746)

Manufactured by Sejoy Biomedical Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The One Step Phencyclidine Rapid Test (Urine) (Model/Catalog Number: Strip,Cassette,Panel,Cup) is a medical device manufactured by Sejoy Biomedical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160509 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Strip,Cassette,Panel,Cup
Product Code / EMDN: W0102160509
Device Name: One Step Oxycodone Rapid Test (Urine)
Database Sync Date: 2026-08-09 18:26:21

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 One Step Phencyclidine Rapid Test (Urine)?

The registered manufacturer of record for One Step Phencyclidine Rapid Test (Urine) is Sejoy Biomedical Co., Ltd..

What is the Primary UDI-DI identifier for One Step Phencyclidine Rapid Test (Urine)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06939663977746.

What classification code is assigned to this device?

This device is registered under product classification code W0102160509.

Similar Classification Devices (W0102160509)

Other Devices by Sejoy Biomedical Co., Ltd.

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