Huka (UDI 08720589794177)

Manufactured by Huka

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Huka (Model/Catalog Number: OR3) is a medical device manufactured by Huka. This product is indexed under FDA Product Code / Category Classification Y121806 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: OR3
Product Code / EMDN: Y121806
Device Name: Orthros 3
Database Sync Date: 2026-08-09 16:28:46

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 Huka?

The registered manufacturer of record for Huka is Huka.

What is the Primary UDI-DI identifier for Huka?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720589794177.

What classification code is assigned to this device?

This device is registered under product classification code Y121806.

Similar Classification Devices (Y121806)

Other Devices by Huka

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