GUDIDData
eudamed_udi Primary ID: 04260179765186

HemoRO 4 ONE (UDI 04260179765186)

Manufactured by DWA Dialyse Wasser Aufbereitungsanlagen GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HemoRO 4 ONE - Primary ID 04260179765186

Device Regulatory Overview

The HemoRO 4 ONE (Model/Catalog Number: 01HRO417DXXXS) is a medical device manufactured by DWA Dialyse Wasser Aufbereitungsanlagen GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Z12099007 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
01HRO417DXXXS
Product Code / EMDN
Z12099007
Device Name
HemoRO 4 ONE
Database Sync Date
2026-08-09 16:29:05

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 HemoRO 4 ONE?

The registered manufacturer of record for HemoRO 4 ONE is DWA Dialyse Wasser Aufbereitungsanlagen GmbH & Co. KG.

What is the Primary UDI-DI identifier for HemoRO 4 ONE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260179765186.

What classification code is assigned to this device?

This device is registered under product classification code Z12099007.

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