gudid Primary ID: 10530

Heimlich valve (UDI 10530)

Manufactured by REDAX SPA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Heimlich valve (Model/Catalog Number: 10530) is a medical device manufactured by REDAX SPA. This product is indexed under FDA Product Code / Category Classification KDQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10530
Product Code / EMDN: KDQ
Device Name: The Heimlich non-return valve is a one-way drainage device which prevents the air reflux towards the patient's chest.
Database Sync Date: 2026-08-09 09:04:33

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 Heimlich valve?

The registered manufacturer of record for Heimlich valve is REDAX SPA.

What is the Primary UDI-DI identifier for Heimlich valve?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10530.

What classification code is assigned to this device?

This device is registered under product classification code KDQ.

Similar Classification Devices (KDQ)

Other Devices by REDAX SPA

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