GUDIDData
gudid Primary ID: HQ-A,1mL/bottle3/box

Hemoglobin Control Solution (UDI HQ-A,1mL/bottle3/box)

Manufactured by Urit Medical Electronic Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hemoglobin Control Solution - Primary ID HQ-A,1mL/bottle3/box

Device Regulatory Overview

The Hemoglobin Control Solution (Model/Catalog Number: HQ-A,1mL/bottle3/box) is a medical device manufactured by Urit Medical Electronic Co., Ltd.. This product is indexed under FDA Product Code / Category Classification GGM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
HQ-A,1mL/bottle3/box
Product Code / EMDN
GGM
Device Name
Database Sync Date
2026-08-09 09:24:45

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 Hemoglobin Control Solution?

The registered manufacturer of record for Hemoglobin Control Solution is Urit Medical Electronic Co., Ltd..

What is the Primary UDI-DI identifier for Hemoglobin Control Solution?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HQ-A,1mL/bottle3/box.

What classification code is assigned to this device?

This device is registered under product classification code GGM.

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