GUDIDData
eudamed_udi Primary ID: 06977667561226

Gauze Cutting (UDI 06977667561226)

Manufactured by Zhejiang Lidesen Medical Instrument Co.,Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gauze Cutting - Primary ID 06977667561226

Device Regulatory Overview

The Gauze Cutting (Model/Catalog Number: 122) is a medical device manufactured by Zhejiang Lidesen Medical Instrument Co.,Ltd. This product is indexed under FDA Product Code / Category Classification M0201010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
122
Product Code / EMDN
M0201010102
Device Name
Gauze Cutting
Database Sync Date
2026-08-09 16:48:03

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 Gauze Cutting?

The registered manufacturer of record for Gauze Cutting is Zhejiang Lidesen Medical Instrument Co.,Ltd.

What is the Primary UDI-DI identifier for Gauze Cutting?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06977667561226.

What classification code is assigned to this device?

This device is registered under product classification code M0201010102.

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