GUDIDData
eudamed_udi Primary ID: 06926365545274

MECO (UDI 06926365545274)

Manufactured by Zhejiang Longterm Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MECO - Primary ID 06926365545274

Device Regulatory Overview

The MECO (Model/Catalog Number: MC020) is a medical device manufactured by Zhejiang Longterm Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M04040201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MC020
Product Code / EMDN
M04040201
Device Name
Alginate dressing
Database Sync Date
2026-08-09 17:12:40

Full Regulatory Attributes

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{
    "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 MECO?

The registered manufacturer of record for MECO is Zhejiang Longterm Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for MECO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06926365545274.

What classification code is assigned to this device?

This device is registered under product classification code M04040201.

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