GUDIDData
gudid Primary ID: 1

Alltest Pregnancy Rapid Combo Test Cassette(Urine/Serum) (UDI 1)

Manufactured by Hangzhou AllTest Biotech Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alltest Pregnancy Rapid Combo Test Cassette(Urine/Serum) - Primary ID 1

Device Regulatory Overview

The Alltest Pregnancy Rapid Combo Test Cassette(Urine/Serum) (Model/Catalog Number: 1) is a medical device manufactured by Hangzhou AllTest Biotech 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
1
Product Code / EMDN
JHI
Device Name
25T(for FDA POC)
Database Sync Date
2026-08-09 09:04:58

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 Alltest Pregnancy Rapid Combo Test Cassette(Urine/Serum)?

The registered manufacturer of record for Alltest Pregnancy Rapid Combo Test Cassette(Urine/Serum) is Hangzhou AllTest Biotech Co., Ltd..

What is the Primary UDI-DI identifier for Alltest Pregnancy Rapid Combo Test Cassette(Urine/Serum)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.

What classification code is assigned to this device?

This device is registered under product classification code JHI.

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