gudid Primary ID: Pro System

FastPack Pro System (UDI Pro System)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The FastPack Pro System (Model/Catalog Number: Pro System) is a medical device manufactured by QUALIGEN INC.. This product is indexed under FDA Product Code / Category Classification JJQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Pro System
Product Code / EMDN: JJQ
Device Name: RoHS Compliant 7-chamber FastPack System
Database Sync Date: 2026-08-09 09:40:11

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 FastPack Pro System?

The registered manufacturer of record for FastPack Pro System is QUALIGEN INC..

What is the Primary UDI-DI identifier for FastPack Pro System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Pro System.

What classification code is assigned to this device?

This device is registered under product classification code JJQ.

Similar Classification Devices (JJQ)

Other Devices by QUALIGEN INC.

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