gudid Primary ID: AR2-042-01

Arch Assembly (UDI AR2-042-01)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Arch Assembly (Model/Catalog Number: AR2-042-01) 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: AR2-042-01
Product Code / EMDN: FOX
Device Name: ASSEMBLY, ACCESSORY ARCH, TS SLED
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 Arch Assembly?

The registered manufacturer of record for Arch Assembly is LIFEPORT, LLC.

What is the Primary UDI-DI identifier for Arch Assembly?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AR2-042-01.

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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