eudamed_udi Primary ID: 06942468134573

OVU TEST (UDI 06942468134573)

Manufactured by Core Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The OVU TEST (Model/Catalog Number: ACK21003-S05-011) is a medical device manufactured by Core Technology 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: ACK21003-S05-011
Product Code / EMDN: W0102160304
Device Name: LH Ovulation Tests
Database Sync Date: 2026-08-09 16:29:01

Full Regulatory Attributes

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{
    "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 OVU TEST?

The registered manufacturer of record for OVU TEST is Core Technology Co., Ltd..

What is the Primary UDI-DI identifier for OVU TEST?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942468134573.

What classification code is assigned to this device?

This device is registered under product classification code W0102160304.

Similar Classification Devices (W0102160304)

Other Devices by Core Technology Co., Ltd.

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