gudid Primary ID: UHI-4

HIGH FLOW INSUFFLATION UNIT (UDI UHI-4)

Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The HIGH FLOW INSUFFLATION UNIT (Model/Catalog Number: UHI-4) is a medical device manufactured by OLYMPUS MEDICAL SYSTEMS CORP.. This product is indexed under FDA Product Code / Category Classification FCX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: UHI-4
Product Code / EMDN: FCX
Device Name: "UHI-4 45L HIGHFLOW INSUFFLATION UNIT"
Database Sync Date: 2026-08-09 09:46:01

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 HIGH FLOW INSUFFLATION UNIT?

The registered manufacturer of record for HIGH FLOW INSUFFLATION UNIT is OLYMPUS MEDICAL SYSTEMS CORP..

What is the Primary UDI-DI identifier for HIGH FLOW INSUFFLATION UNIT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UHI-4.

What classification code is assigned to this device?

This device is registered under product classification code FCX.

Similar Classification Devices (FCX)

Other Devices by OLYMPUS MEDICAL SYSTEMS CORP.

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