GUDIDData
eudamed_udi Primary ID: 06975488440966

Fully automatic multifunctional gel imaging system (UDI 06975488440966)

Manufactured by Infitek Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fully automatic multifunctional gel imaging system - Primary ID 06975488440966

Device Regulatory Overview

The Fully automatic multifunctional gel imaging system (Model/Catalog Number: GEP-GD600MF) is a medical device manufactured by Infitek Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W020105019002 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
GEP-GD600MF
Product Code / EMDN
W020105019002
Device Name
Gel Imaging System
Database Sync Date
2026-08-09 16:51:52

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 Fully automatic multifunctional gel imaging system?

The registered manufacturer of record for Fully automatic multifunctional gel imaging system is Infitek Co., Ltd..

What is the Primary UDI-DI identifier for Fully automatic multifunctional gel imaging system?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975488440966.

What classification code is assigned to this device?

This device is registered under product classification code W020105019002.

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