GUDIDData
eudamed_udi Primary ID: 04719872280491

Diafit/Plus Comfort Elektronski Nosni aspirator (UDI 04719872280491)

Manufactured by Asia Connection Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Diafit/Plus Comfort Elektronski Nosni aspirator - Primary ID 04719872280491

Device Regulatory Overview

The Diafit/Plus Comfort Elektronski Nosni aspirator (Model/Catalog Number: ME8202X-Diafit) is a medical device manufactured by Asia Connection Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R05010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ME8202X-Diafit
Product Code / EMDN
R05010301
Device Name
Powered Nasal Aspirator
Database Sync Date
2026-08-09 16:51:59

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 Diafit/Plus Comfort Elektronski Nosni aspirator?

The registered manufacturer of record for Diafit/Plus Comfort Elektronski Nosni aspirator is Asia Connection Co., Ltd..

What is the Primary UDI-DI identifier for Diafit/Plus Comfort Elektronski Nosni aspirator?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719872280491.

What classification code is assigned to this device?

This device is registered under product classification code R05010301.

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