gudid Primary ID: BY-GM224

Gemini (UDI BY-GM224)

Manufactured by Beyond International Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Gemini (Model/Catalog Number: BY-GM224) is a medical device manufactured by Beyond International Inc.. This product is indexed under FDA Product Code / Category Classification EEG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: BY-GM224
Product Code / EMDN: EEG
Device Name
Database Sync Date: 2026-08-09 09:49:26

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 Gemini?

The registered manufacturer of record for Gemini is Beyond International Inc..

What is the Primary UDI-DI identifier for Gemini?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BY-GM224.

What classification code is assigned to this device?

This device is registered under product classification code EEG.

Similar Classification Devices (EEG)

Other Devices by Beyond International Inc.

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