eudamed_udi Primary ID: 76936662650709

Nonsterile Gauze Rolls (UDI 76936662650709)

Manufactured by Kingstar Medical (Xianning) Co., LTD

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Nonsterile Gauze Rolls (Model/Catalog Number: C006015) is a medical device manufactured by Kingstar Medical (Xianning) 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: C006015
Product Code / EMDN: M0201010102
Device Name: Nonsterile Gauze Rolls
Database Sync Date: 2026-08-09 16:50:29

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 Nonsterile Gauze Rolls?

The registered manufacturer of record for Nonsterile Gauze Rolls is Kingstar Medical (Xianning) Co., LTD.

What is the Primary UDI-DI identifier for Nonsterile Gauze Rolls?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 76936662650709.

What classification code is assigned to this device?

This device is registered under product classification code M0201010102.

Similar Classification Devices (M0201010102)

Other Devices by Kingstar Medical (Xianning) Co., LTD

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