gudid Primary ID: 100-5459-03

Folding Transport Sled (FTS) (UDI 100-5459-03)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Folding Transport Sled (FTS) (Model/Catalog Number: 100-5459-03) is a medical device manufactured by LIFEPORT, LLC. This product is indexed under FDA Product Code / Category Classification FPP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 100-5459-03
Product Code / EMDN: FPP
Device Name: ASSEMBLY - FOLDING TRANSPORT SLED (FTS) * 27.70 TALL WITH ALIGNMENT WEDGE
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 Folding Transport Sled (FTS)?

The registered manufacturer of record for Folding Transport Sled (FTS) is LIFEPORT, LLC.

What is the Primary UDI-DI identifier for Folding Transport Sled (FTS)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 100-5459-03.

What classification code is assigned to this device?

This device is registered under product classification code FPP.

Similar Classification Devices (FPP)

Other Devices by LIFEPORT, LLC

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