GUDIDData
eudamed_udi Primary ID: 06974521004493

tPAIC Assay kit CLIA (UDI 06974521004493)

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 tPAIC Assay kit CLIA - Primary ID 06974521004493

Device Regulatory Overview

The tPAIC Assay kit CLIA (Model/Catalog Number: SUPM085072) is a medical device manufactured by Shenzhen Superbio Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0103020506 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SUPM085072
Product Code / EMDN
W0103020506
Device Name
tPAIC Assay kit CLIA
Database Sync Date
2026-08-09 16:28:46

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 tPAIC Assay kit CLIA?

The registered manufacturer of record for tPAIC Assay kit CLIA is Shenzhen Superbio Technology Co.,Ltd..

What is the Primary UDI-DI identifier for tPAIC Assay kit CLIA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974521004493.

What classification code is assigned to this device?

This device is registered under product classification code W0103020506.

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