gudid Primary ID: 24100

Sample: Opti-Tatt (UDI 24100)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Sample: Opti-Tatt (Model/Catalog Number: 24100) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification FZZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 24100
Product Code / EMDN: FZZ
Device Name: Opti-Tatt Sample - 2 Dot, 2 Crosshair, 2 Field Border
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 Sample: Opti-Tatt?

The registered manufacturer of record for Sample: Opti-Tatt is Bionix, LLC.

What is the Primary UDI-DI identifier for Sample: Opti-Tatt?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 24100.

What classification code is assigned to this device?

This device is registered under product classification code FZZ.

Similar Classification Devices (FZZ)

Other Devices by Bionix, LLC

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