gudid Primary ID: 603-019175

Dimora (UDI 603-019175)

Manufactured by Winner Medical Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Dimora (Model/Catalog Number: 603-019175) is a medical device manufactured by Winner Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification FRO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 603-019175
Product Code / EMDN: FRO
Device Name: Skin and Wound Cleanser
Database Sync Date: 2026-08-09 09:11:11

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 Dimora?

The registered manufacturer of record for Dimora is Winner Medical Co., Ltd..

What is the Primary UDI-DI identifier for Dimora?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 603-019175.

What classification code is assigned to this device?

This device is registered under product classification code FRO.

Similar Classification Devices (FRO)

Other Devices by Winner Medical Co., Ltd.

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