gudid Primary ID: Lvivo_Seamless

Lvivo Seamless (UDI Lvivo_Seamless)

Manufactured by DIA IMAGING ANALYSIS LTD

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lvivo Seamless (Model/Catalog Number: Lvivo_Seamless) is a medical device manufactured by DIA IMAGING ANALYSIS LTD. This product is indexed under FDA Product Code / Category Classification QIH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Lvivo_Seamless
Product Code / EMDN: QIH
Device Name
Database Sync Date: 2026-08-09 09:18:16

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 Lvivo Seamless?

The registered manufacturer of record for Lvivo Seamless is DIA IMAGING ANALYSIS LTD.

What is the Primary UDI-DI identifier for Lvivo Seamless?

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

What classification code is assigned to this device?

This device is registered under product classification code QIH.

Similar Classification Devices (QIH)

Other Devices by DIA IMAGING ANALYSIS LTD

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