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eudamed_udi Primary ID: 06942013206328

Absorbent Non-Woven Compress (UDI 06942013206328)

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 Absorbent Non-Woven Compress - Primary ID 06942013206328

Device Regulatory Overview

The Absorbent Non-Woven Compress (Model/Catalog Number: 2090000037 for Reflex) is a medical device manufactured by Hubei V-Medical Products Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification M040301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2090000037 for Reflex
Product Code / EMDN
M040301
Device Name
Eye Pads 眼垫
Database Sync Date
2026-08-09 16:59:50

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 Absorbent Non-Woven Compress?

The registered manufacturer of record for Absorbent Non-Woven Compress is Hubei V-Medical Products Co.,Ltd..

What is the Primary UDI-DI identifier for Absorbent Non-Woven Compress?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942013206328.

What classification code is assigned to this device?

This device is registered under product classification code M040301.

Similar Classification Devices (M040301)

Other Devices by Hubei V-Medical Products Co.,Ltd.

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