gudid Primary ID: P6601-01-088

Patient Loading Utility System (PLUS) (UDI P6601-01-088)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Patient Loading Utility System (PLUS) (Model/Catalog Number: P6601-01-088) is a medical device manufactured by LIFEPORT, LLC. This product is indexed under FDA Product Code / Category Classification FOX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: P6601-01-088
Product Code / EMDN: FOX
Device Name: PLUS, 66 IN STRUCTURE * PATIENT LOADING UTILITY SYSTEM
Database Sync Date: 2026-08-09 09:10:00

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 Patient Loading Utility System (PLUS)?

The registered manufacturer of record for Patient Loading Utility System (PLUS) is LIFEPORT, LLC.

What is the Primary UDI-DI identifier for Patient Loading Utility System (PLUS)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P6601-01-088.

What classification code is assigned to this device?

This device is registered under product classification code FOX.

Similar Classification Devices (FOX)

Other Devices by LIFEPORT, LLC

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