gudid Primary ID: PR-V614M

Single Use 2-Lumen Cannula V (UDI PR-V614M)

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 Single Use 2-Lumen Cannula V (Model/Catalog Number: PR-V614M) is a medical device manufactured by OLYMPUS MEDICAL SYSTEMS CORP.. This product is indexed under FDA Product Code / Category Classification ODD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PR-V614M
Product Code / EMDN: ODD
Device Name: Single Use 2-Lumen Cannula V
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 Single Use 2-Lumen Cannula V?

The registered manufacturer of record for Single Use 2-Lumen Cannula V is OLYMPUS MEDICAL SYSTEMS CORP..

What is the Primary UDI-DI identifier for Single Use 2-Lumen Cannula V?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PR-V614M.

What classification code is assigned to this device?

This device is registered under product classification code ODD.

Similar Classification Devices (ODD)

Other Devices by OLYMPUS MEDICAL SYSTEMS CORP.

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