GUDIDData
gudid Primary ID: HW-F7

Breathe Pure (UDI HW-F7)

Manufactured by Dongguan SIMZO Electronic Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Breathe Pure - Primary ID HW-F7

Device Regulatory Overview

The Breathe Pure (Model/Catalog Number: HW-F7) is a medical device manufactured by Dongguan SIMZO Electronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification FLL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
HW-F7
Product Code / EMDN
FLL
Device Name
Database Sync Date
2026-08-09 09:17:07

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Breathe Pure?

The registered manufacturer of record for Breathe Pure is Dongguan SIMZO Electronic Technology Co., Ltd..

What is the Primary UDI-DI identifier for Breathe Pure?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HW-F7.

What classification code is assigned to this device?

This device is registered under product classification code FLL.

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