GUDIDData
gudid Primary ID: 0404-0301-04-02

ServiPlex (UDI 0404-0301-04-02)

Manufactured by LIFEPORT, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ServiPlex - Primary ID 0404-0301-04-02

Device Regulatory Overview

The ServiPlex (Model/Catalog Number: 0404-0301-04-02) 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
0404-0301-04-02
Product Code / EMDN
FOX
Device Name
ASSEMBLY - SERVIPLEX
Database Sync Date
2026-08-09 09:10:00

Full Regulatory Attributes

🔒 Token Gated
{
    "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 ServiPlex?

The registered manufacturer of record for ServiPlex is LIFEPORT, LLC.

What is the Primary UDI-DI identifier for ServiPlex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0404-0301-04-02.

What classification code is assigned to this device?

This device is registered under product classification code FOX.

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