AVIEW (UDI 1.1)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AVIEW (Model/Catalog Number: 1.1) is a medical device manufactured by CORELINE SOFT CO.,LTD.. This product is indexed under FDA Product Code / Category Classification QIH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1.1
Product Code / EMDN: QIH
Device Name
Database Sync Date: 2026-08-09 09:28:52

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 AVIEW?

The registered manufacturer of record for AVIEW is CORELINE SOFT CO.,LTD..

What is the Primary UDI-DI identifier for AVIEW?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.1.

What classification code is assigned to this device?

This device is registered under product classification code QIH.

Similar Classification Devices (QIH)

Other Devices by CORELINE SOFT CO.,LTD.

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