gudid Primary ID: 2650

Lighted Microsuction System (UDI 2650)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lighted Microsuction System (Model/Catalog Number: 2650) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification KDQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2650
Product Code / EMDN: KDQ
Device Name: Lighted Microsuction System Starter Pack
Database Sync Date: 2026-08-09 09:04:11

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 Lighted Microsuction System?

The registered manufacturer of record for Lighted Microsuction System is Bionix, LLC.

What is the Primary UDI-DI identifier for Lighted Microsuction System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2650.

What classification code is assigned to this device?

This device is registered under product classification code KDQ.

Similar Classification Devices (KDQ)

Other Devices by Bionix, LLC

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