GUDIDData
eudamed_udi Primary ID: 06921963711236

Opiate Saliva Test Card (UDI 06921963711236)

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 Opiate Saliva Test Card - Primary ID 06921963711236

Device Regulatory Overview

The Opiate Saliva Test Card (Model/Catalog Number: 1L11C5) is a medical device manufactured by Xiamen Boson Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160508 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1L11C5
Product Code / EMDN
W0102160508
Device Name
Opiate Saliva Test Card
Database Sync Date
2026-08-09 18:43:20

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Opiate Saliva Test Card?

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

What is the Primary UDI-DI identifier for Opiate Saliva Test Card?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06921963711236.

What classification code is assigned to this device?

This device is registered under product classification code W0102160508.

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