GUDIDData
eudamed_udi Primary ID: 06933260205554

FSH Rapid Quantitative Test (Chemiluminescence Immunoassay) (UDI 06933260205554)

Manufactured by Xiamen Biotime Biotechnology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FSH Rapid Quantitative Test (Chemiluminescence Immunoassay) - Primary ID 06933260205554

Device Regulatory Overview

The FSH Rapid Quantitative Test (Chemiluminescence Immunoassay) (Model/Catalog Number: BT0503002) is a medical device manufactured by Xiamen Biotime Biotechnology 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
BT0503002
Product Code / EMDN
W0102160301
Device Name
FSH Rapid Quantitative Test (Chemiluminescence Immunoassay)
Database Sync Date
2026-08-09 18:03:46

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 Rapid Quantitative Test (Chemiluminescence Immunoassay)?

The registered manufacturer of record for FSH Rapid Quantitative Test (Chemiluminescence Immunoassay) is Xiamen Biotime Biotechnology Co., Ltd..

What is the Primary UDI-DI identifier for FSH Rapid Quantitative Test (Chemiluminescence Immunoassay)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06933260205554.

What classification code is assigned to this device?

This device is registered under product classification code W0102160301.

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