GUDIDData
eudamed_udi Primary ID: 06957683732473

TESTEO (UDI 06957683732473)

Manufactured by Gaobeidian PRISES Biotechnology Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TESTEO - Primary ID 06957683732473

Device Regulatory Overview

The TESTEO (Model/Catalog Number: LHM60B-7T) is a medical device manufactured by Gaobeidian PRISES Biotechnology Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0102160304 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
LHM60B-7T
Product Code / EMDN
W0102160304
Device Name
One Step LH Ovulation Test
Database Sync Date
2026-08-09 16:28:50

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 TESTEO?

The registered manufacturer of record for TESTEO is Gaobeidian PRISES Biotechnology Co., Ltd.

What is the Primary UDI-DI identifier for TESTEO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06957683732473.

What classification code is assigned to this device?

This device is registered under product classification code W0102160304.

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