gudid Primary ID: KD-7920

ARRIGO PROFESSIONAL SUPPLIES LLC (UDI KD-7920)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ARRIGO PROFESSIONAL SUPPLIES LLC (Model/Catalog Number: KD-7920) is a medical device manufactured by Andon Health Co., Ltd.. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: KD-7920
Product Code / EMDN: DXN
Device Name
Database Sync Date: 2026-08-09 09:37:38

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 ARRIGO PROFESSIONAL SUPPLIES LLC?

The registered manufacturer of record for ARRIGO PROFESSIONAL SUPPLIES LLC is Andon Health Co., Ltd..

What is the Primary UDI-DI identifier for ARRIGO PROFESSIONAL SUPPLIES LLC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KD-7920.

What classification code is assigned to this device?

This device is registered under product classification code DXN.

Similar Classification Devices (DXN)

Other Devices by Andon Health Co., Ltd.

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