GUDIDData
eudamed_udi Primary ID: 06942013210431

EURODIST TRIANGULAR BANDAGE NON-WOVEN DIN (UDI 06942013210431)

Manufactured by Hubei V-Medical Products Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EURODIST TRIANGULAR BANDAGE NON-WOVEN DIN - Primary ID 06942013210431

Device Regulatory Overview

The EURODIST TRIANGULAR BANDAGE NON-WOVEN DIN (Model/Catalog Number: 41112) is a medical device manufactured by Hubei V-Medical Products Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification M03030199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
41112
Product Code / EMDN
M03030199
Device Name
Triangular bandage δΈ‰θ§’η»·εΈ¦
Database Sync Date
2026-08-09 16:30:17

Full Regulatory Attributes

πŸ”’ 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 EURODIST TRIANGULAR BANDAGE NON-WOVEN DIN?

The registered manufacturer of record for EURODIST TRIANGULAR BANDAGE NON-WOVEN DIN is Hubei V-Medical Products Co.,Ltd..

What is the Primary UDI-DI identifier for EURODIST TRIANGULAR BANDAGE NON-WOVEN DIN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942013210431.

What classification code is assigned to this device?

This device is registered under product classification code M03030199.

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