GUDIDData
eudamed_udi Primary ID: D-FSH-D06aFR

FSH Test Kit FIA (UDI D-FSH-D06aFR)

Manufactured by Hangzhou Aichek Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FSH Test Kit FIA - Primary ID D-FSH-D06aFR

Device Regulatory Overview

The FSH Test Kit FIA (Model/Catalog Number: FSH-D06a) is a medical device manufactured by Hangzhou Aichek Medical Technology 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
FSH-D06a
Product Code / EMDN
W0102160301
Device Name
FSH Test Kit FIA
Database Sync Date
2026-08-09 17:07:58

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 FSH Test Kit FIA?

The registered manufacturer of record for FSH Test Kit FIA is Hangzhou Aichek Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for FSH Test Kit FIA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-FSH-D06aFR.

What classification code is assigned to this device?

This device is registered under product classification code W0102160301.

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