GUDIDData
eudamed_udi Primary ID: 06974521007746

S-Trust Fentanyl Urine Detection Kit (Fluorescence Immunochromatographic Assay) (UDI 06974521007746)

Manufactured by Shenzhen Superbio Technology Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for S-Trust Fentanyl Urine Detection Kit (Fluorescence Immunochromatographic Assay) - Primary ID 06974521007746

Device Regulatory Overview

The S-Trust Fentanyl Urine Detection Kit (Fluorescence Immunochromatographic Assay) (Model/Catalog Number: SUPG352025) is a medical device manufactured by Shenzhen Superbio Technology 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
SUPG352025
Product Code / EMDN
W0102160508
Device Name
S-Trust Fentanyl Urine Detection Kit (Fluorescence Immunochromatographic Assay)
Database Sync Date
2026-08-09 16:47:17

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 S-Trust Fentanyl Urine Detection Kit (Fluorescence Immunochromatographic Assay)?

The registered manufacturer of record for S-Trust Fentanyl Urine Detection Kit (Fluorescence Immunochromatographic Assay) is Shenzhen Superbio Technology Co.,Ltd..

What is the Primary UDI-DI identifier for S-Trust Fentanyl Urine Detection Kit (Fluorescence Immunochromatographic Assay)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974521007746.

What classification code is assigned to this device?

This device is registered under product classification code W0102160508.

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