gudid Primary ID: ASTRD292.MVU

UNBRANDED (UDI ASTRD292.MVU)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The UNBRANDED (Model/Catalog Number: ASTRD292.MVU) is a medical device manufactured by FGX INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification HOI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ASTRD292.MVU
Product Code / EMDN: HOI
Device Name
Database Sync Date: 2026-08-09 09:00:32

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 UNBRANDED?

The registered manufacturer of record for UNBRANDED is FGX INTERNATIONAL INC..

What is the Primary UDI-DI identifier for UNBRANDED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ASTRD292.MVU.

What classification code is assigned to this device?

This device is registered under product classification code HOI.

Similar Classification Devices (HOI)

Other Devices by FGX INTERNATIONAL INC.

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