gudid Primary ID: HP-HUGO

HP-HUGO Automatic Tissue Processor (UDI HP-HUGO)

Manufactured by Dakewe (Shenzhen) Medical Equipment Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The HP-HUGO Automatic Tissue Processor (Model/Catalog Number: HP-HUGO) is a medical device manufactured by Dakewe (Shenzhen) Medical Equipment Co., Ltd.. This product is indexed under FDA Product Code / Category Classification IEO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: HP-HUGO
Product Code / EMDN: IEO
Device Name
Database Sync Date: 2026-08-09 09:06:44

Full Regulatory Attributes

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{
    "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 HP-HUGO Automatic Tissue Processor?

The registered manufacturer of record for HP-HUGO Automatic Tissue Processor is Dakewe (Shenzhen) Medical Equipment Co., Ltd..

What is the Primary UDI-DI identifier for HP-HUGO Automatic Tissue Processor?

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

What classification code is assigned to this device?

This device is registered under product classification code IEO.

Similar Classification Devices (IEO)

Other Devices by Dakewe (Shenzhen) Medical Equipment Co., Ltd.

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