GUDIDData
eudamed_udi Primary ID: 06954414751871

Akso SARS-CoV-2/FluA/FluB Real-time RT-PCR Kit (UDI 06954414751871)

Manufactured by Getein Biotech, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Akso SARS-CoV-2/FluA/FluB Real-time RT-PCR Kit - Primary ID 06954414751871

Device Regulatory Overview

The Akso SARS-CoV-2/FluA/FluB Real-time RT-PCR Kit (Model/Catalog Number: RT6005) is a medical device manufactured by Getein Biotech, Inc.. This product is indexed under FDA Product Code / Category Classification W0105070304 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RT6005
Product Code / EMDN
W0105070304
Device Name
Akso SARS-CoV-2/FluA/FluB Real-time RT-PCR Kit
Database Sync Date
2026-08-09 16:29:04

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 Akso SARS-CoV-2/FluA/FluB Real-time RT-PCR Kit?

The registered manufacturer of record for Akso SARS-CoV-2/FluA/FluB Real-time RT-PCR Kit is Getein Biotech, Inc..

What is the Primary UDI-DI identifier for Akso SARS-CoV-2/FluA/FluB Real-time RT-PCR Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06954414751871.

What classification code is assigned to this device?

This device is registered under product classification code W0105070304.

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