eudamed_udi Primary ID: 06936983120081

FSH Rapid Test Midstream (UDI 06936983120081)

Manufactured by Hangzhou Alltest Biotech.Co.,Ltd.

Data verified against official FDA/EUDAMED records on August 10, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The FSH Rapid Test Midstream (Model/Catalog Number: FFS-103H) is a medical device manufactured by Hangzhou Alltest Biotech.Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FFS-103H
Product Code / EMDN: W0102160301
Device Name: FSH Rapid Test Midstream
Database Sync Date: 2026-08-10 05:06:07

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 FSH Rapid Test Midstream?

The registered manufacturer of record for FSH Rapid Test Midstream is Hangzhou Alltest Biotech.Co.,Ltd..

What is the Primary UDI-DI identifier for FSH Rapid Test Midstream?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936983120081.

What classification code is assigned to this device?

This device is registered under product classification code W0102160301.

Similar Classification Devices (W0102160301)

Other Devices by Hangzhou Alltest Biotech.Co.,Ltd.

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