GUDIDData
eudamed_udi Primary ID: 06921963710253

Rapid Phencyclidine Test Card (UDI 06921963710253)

Manufactured by Xiamen Boson Biotech Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rapid Phencyclidine Test Card - Primary ID 06921963710253

Device Regulatory Overview

The Rapid Phencyclidine Test Card (Model/Catalog Number: 1L13C3) is a medical device manufactured by Xiamen Boson Biotech 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
1L13C3
Product Code / EMDN
W0102160509
Device Name
Rapid Phencyclidine Test Card
Database Sync Date
2026-08-09 17:24:57

Full Regulatory Attributes

๐Ÿ”’ 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 Phencyclidine Test Card?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06921963710253.

What classification code is assigned to this device?

This device is registered under product classification code W0102160509.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint