eudamed_udi Primary ID: 16975743610056

Wound Plaster (UDI 16975743610056)

Manufactured by Changzhou UEKON Healthcare Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Wound Plaster (Model/Catalog Number: YYK011 38mm×19mm) is a medical device manufactured by Changzhou UEKON Healthcare Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M04010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: YYK011 38mm×19mm
Product Code / EMDN: M04010101
Device Name: Wound Plaster
Database Sync Date: 2026-08-09 16:28:47

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 Wound Plaster?

The registered manufacturer of record for Wound Plaster is Changzhou UEKON Healthcare Co., Ltd..

What is the Primary UDI-DI identifier for Wound Plaster?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16975743610056.

What classification code is assigned to this device?

This device is registered under product classification code M04010101.

Similar Classification Devices (M04010101)

Other Devices by Changzhou UEKON Healthcare Co., Ltd.

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