GUDIDData
eudamed_udi Primary ID: 04260338744144

Selbstklebende Wundpflaster (UDI 04260338744144)

Manufactured by Hynaut Health Technology Co., LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Selbstklebende Wundpflaster - Primary ID 04260338744144

Device Regulatory Overview

The Selbstklebende Wundpflaster (Model/Catalog Number: C104) is a medical device manufactured by Hynaut Health Technology Co., LTD. This product is indexed under FDA Product Code / Category Classification M04010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
C104
Product Code / EMDN
M04010102
Device Name
Adhesive Wound plaster
Database Sync Date
2026-08-09 17:05:13

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 Selbstklebende Wundpflaster?

The registered manufacturer of record for Selbstklebende Wundpflaster is Hynaut Health Technology Co., LTD.

What is the Primary UDI-DI identifier for Selbstklebende Wundpflaster?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260338744144.

What classification code is assigned to this device?

This device is registered under product classification code M04010102.

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