eudamed_udi Primary ID: 08432229175221

ESPARADRAPO DE TEJIDO NO TEJIDO EN ROLLO (UDI 08432229175221)

Manufactured by Zhende Medical Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The ESPARADRAPO DE TEJIDO NO TEJIDO EN ROLLO (Model/Catalog Number: NT2009.2) is a medical device manufactured by Zhende Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M04010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: NT2009.2
Product Code / EMDN: M04010201
Device Name: Medical dressing roll
Database Sync Date: 2026-08-09 16:48:34

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 ESPARADRAPO DE TEJIDO NO TEJIDO EN ROLLO?

The registered manufacturer of record for ESPARADRAPO DE TEJIDO NO TEJIDO EN ROLLO is Zhende Medical Co., Ltd..

What is the Primary UDI-DI identifier for ESPARADRAPO DE TEJIDO NO TEJIDO EN ROLLO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08432229175221.

What classification code is assigned to this device?

This device is registered under product classification code M04010201.

Similar Classification Devices (M04010201)

Other Devices by Zhende Medical Co., Ltd.

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