GUDIDData
eudamed_udi Primary ID: 06953102631853

Wound Plaster (UDI 06953102631853)

Manufactured by Taizhou Xinkang Medical Materials Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wound Plaster - Primary ID 06953102631853

Device Regulatory Overview

The Wound Plaster (Model/Catalog Number: TX1214) is a medical device manufactured by Taizhou Xinkang Medical Materials 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
TX1214
Product Code / EMDN
M04010101
Device Name
Wound Plaster
Database Sync Date
2026-08-09 18:12:27

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 Wound Plaster?

The registered manufacturer of record for Wound Plaster is Taizhou Xinkang Medical Materials 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 06953102631853.

What classification code is assigned to this device?

This device is registered under product classification code M04010101.

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