GUDIDData
gudid Primary ID: HCP-80B

Haier Biomedical (UDI HCP-80B)

Manufactured by Qingdao Haier Biomedical Technology Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Haier Biomedical - Primary ID HCP-80B

Device Regulatory Overview

The Haier Biomedical (Model/Catalog Number: HCP-80B) is a medical device manufactured by Qingdao Haier Biomedical Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification JTQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
HCP-80B
Product Code / EMDN
JTQ
Device Name
Carbon dioxide laboratory incubator
Database Sync Date
2026-08-09 09:06:38

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 Haier Biomedical?

The registered manufacturer of record for Haier Biomedical is Qingdao Haier Biomedical Technology Co.,Ltd..

What is the Primary UDI-DI identifier for Haier Biomedical?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HCP-80B.

What classification code is assigned to this device?

This device is registered under product classification code JTQ.

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