GUDIDData
eudamed_udi Primary ID: 06975662250015

HEKA TRIANGULAR BANDAGE (UDI 06975662250015)

Manufactured by Suzhou Vicon Industrial CO., LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HEKA TRIANGULAR BANDAGE - Primary ID 06975662250015

Device Regulatory Overview

The HEKA TRIANGULAR BANDAGE (Model/Catalog Number: HD0600) is a medical device manufactured by Suzhou Vicon Industrial CO., LTD.. This product is indexed under FDA Product Code / Category Classification M030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
HD0600
Product Code / EMDN
M030101
Device Name
I
Database Sync Date
2026-08-09 18:55:31

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 HEKA TRIANGULAR BANDAGE?

The registered manufacturer of record for HEKA TRIANGULAR BANDAGE is Suzhou Vicon Industrial CO., LTD..

What is the Primary UDI-DI identifier for HEKA TRIANGULAR BANDAGE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975662250015.

What classification code is assigned to this device?

This device is registered under product classification code M030101.

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