GUDIDData
eudamed_udi Primary ID: 06975706484857

Non-woven plaster 20cmx10m 1 roll (UDI 06975706484857)

Manufactured by Bestreat Safety & First Aid Solution Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Non-woven plaster 20cmx10m 1 roll - Primary ID 06975706484857

Device Regulatory Overview

The Non-woven plaster 20cmx10m 1 roll (Model/Catalog Number: 1455-20X10) is a medical device manufactured by Bestreat Safety & First Aid Solution 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
1455-20X10
Product Code / EMDN
M040301
Device Name
Absorbent Nonwoven Compress(Non-sterile)
Database Sync Date
2026-08-09 16:29:07

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 Non-woven plaster 20cmx10m 1 roll?

The registered manufacturer of record for Non-woven plaster 20cmx10m 1 roll is Bestreat Safety & First Aid Solution Co., Ltd..

What is the Primary UDI-DI identifier for Non-woven plaster 20cmx10m 1 roll?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975706484857.

What classification code is assigned to this device?

This device is registered under product classification code M040301.

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