GUDIDData
gudid Primary ID: Midstream,5PCS/BOX

HCG Home Use Pregnancy Test Midstream (Colloidal Gold) (UDI Midstream,5PCS/BOX)

Manufactured by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HCG Home Use Pregnancy Test Midstream (Colloidal Gold) - Primary ID Midstream,5PCS/BOX

Device Regulatory Overview

The HCG Home Use Pregnancy Test Midstream (Colloidal Gold) (Model/Catalog Number: Midstream,5PCS/BOX) is a medical device manufactured by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD. This product is indexed under FDA Product Code / Category Classification JHI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Midstream,5PCS/BOX
Product Code / EMDN
JHI
Device Name
The HCG Home Use Pregnancy Test Midstream (Colloidal Gold) is a rapid chromatographic immunoassay for thequalitative detection of human chorionic gonadotropin (hCG) in urine to aid in the early detection of pregnancy.
Database Sync Date
2026-08-09 09:05:25

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 HCG Home Use Pregnancy Test Midstream (Colloidal Gold)?

The registered manufacturer of record for HCG Home Use Pregnancy Test Midstream (Colloidal Gold) is ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD.

What is the Primary UDI-DI identifier for HCG Home Use Pregnancy Test Midstream (Colloidal Gold)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Midstream,5PCS/BOX.

What classification code is assigned to this device?

This device is registered under product classification code JHI.

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