eudamed_udi Primary ID: 06940181416082

Splint (UDI 06940181416082)

Manufactured by Zhuozhou Huanuo Life-Saving Equipment Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Splint (Model/Catalog Number: 310mm×110mm) is a medical device manufactured by Zhuozhou Huanuo Life-Saving Equipment Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification M03050299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 310mm×110mm
Product Code / EMDN: M03050299
Device Name: Splint
Database Sync Date: 2026-08-09 16:45:56

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 Splint?

The registered manufacturer of record for Splint is Zhuozhou Huanuo Life-Saving Equipment Co.,Ltd..

What is the Primary UDI-DI identifier for Splint?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06940181416082.

What classification code is assigned to this device?

This device is registered under product classification code M03050299.

Similar Classification Devices (M03050299)

Other Devices by Zhuozhou Huanuo Life-Saving Equipment Co.,Ltd.

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