gudid Primary ID: 23301

ClearLook Sample Pack-Curettes & Light Source (UDI 23301)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ClearLook Sample Pack-Curettes & Light Source (Model/Catalog Number: 23301) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification JYG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 23301
Product Code / EMDN: JYG
Device Name: ClearLook Sample Pack-Curettes & Light Source
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 ClearLook Sample Pack-Curettes & Light Source?

The registered manufacturer of record for ClearLook Sample Pack-Curettes & Light Source is Bionix, LLC.

What is the Primary UDI-DI identifier for ClearLook Sample Pack-Curettes & Light Source?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 23301.

What classification code is assigned to this device?

This device is registered under product classification code JYG.

Similar Classification Devices (JYG)

Other Devices by Bionix, LLC

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