eudamed_udi Primary ID: 06909620251288

Telano Pregnancy Test (UDI 06909620251288)

Manufactured by W.H.P.M. Bioresearch & Technology Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Telano Pregnancy Test (Model/Catalog Number: WH-FT-S3943P07) is a medical device manufactured by W.H.P.M. Bioresearch & Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: WH-FT-S3943P07
Product Code / EMDN: W0102160302
Device Name: Pregnancy Tests
Database Sync Date: 2026-08-09 16:29:33

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 Telano Pregnancy Test?

The registered manufacturer of record for Telano Pregnancy Test is W.H.P.M. Bioresearch & Technology Co., Ltd..

What is the Primary UDI-DI identifier for Telano Pregnancy Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06909620251288.

What classification code is assigned to this device?

This device is registered under product classification code W0102160302.

Similar Classification Devices (W0102160302)

Other Devices by W.H.P.M. Bioresearch & Technology Co., Ltd.

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