GUDIDData
gudid Primary ID: A80

LOOKEE AscleTrack Urine Test Analyzer (UDI A80)

Manufactured by Kunming Lianen Biotechnology Co., LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LOOKEE AscleTrack Urine Test Analyzer - Primary ID A80

Device Regulatory Overview

The LOOKEE AscleTrack Urine Test Analyzer (Model/Catalog Number: A80) is a medical device manufactured by Kunming Lianen Biotechnology Co., LTD. This product is indexed under FDA Product Code / Category Classification KQO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
A80
Product Code / EMDN
KQO
Device Name
Database Sync Date
2026-08-09 09:06:41

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 LOOKEE AscleTrack Urine Test Analyzer?

The registered manufacturer of record for LOOKEE AscleTrack Urine Test Analyzer is Kunming Lianen Biotechnology Co., LTD.

What is the Primary UDI-DI identifier for LOOKEE AscleTrack Urine Test Analyzer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A80.

What classification code is assigned to this device?

This device is registered under product classification code KQO.

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