gudid Primary ID: UA8069

URIC ACID (UA) (UDI UA8069)

Manufactured by RANDOX LABORATORIES LIMITED

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

Scannable UDI-DI Representation

Device Regulatory Overview

The URIC ACID (UA) (Model/Catalog Number: UA8069) is a medical device manufactured by RANDOX LABORATORIES LIMITED. This product is indexed under FDA Product Code / Category Classification KNK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: UA8069
Product Code / EMDN: KNK
Device Name
Database Sync Date: 2026-08-09 09:39:53

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 URIC ACID (UA)?

The registered manufacturer of record for URIC ACID (UA) is RANDOX LABORATORIES LIMITED.

What is the Primary UDI-DI identifier for URIC ACID (UA)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UA8069.

What classification code is assigned to this device?

This device is registered under product classification code KNK.

Similar Classification Devices (KNK)

Other Devices by RANDOX LABORATORIES LIMITED

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