gudid Primary ID: 237-99

URIC ACID-SL Assay (UDI 237-99)

Manufactured by Sekisui Diagnostics, LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The URIC ACID-SL Assay (Model/Catalog Number: 237-99) is a medical device manufactured by Sekisui Diagnostics, LLC. This product is indexed under FDA Product Code / Category Classification KNK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 237-99
Product Code / EMDN: KNK
Device Name
Database Sync Date: 2026-08-09 09:50:05

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-SL Assay?

The registered manufacturer of record for URIC ACID-SL Assay is Sekisui Diagnostics, LLC.

What is the Primary UDI-DI identifier for URIC ACID-SL Assay?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 237-99.

What classification code is assigned to this device?

This device is registered under product classification code KNK.

Similar Classification Devices (KNK)

Other Devices by Sekisui Diagnostics, LLC

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