gudid Primary ID: 22-18-0100

VACUTRON (UDI 22-18-0100)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The VACUTRON (Model/Catalog Number: 22-18-0100) is a medical device manufactured by Allied Medical, LLC. This product is indexed under FDA Product Code / Category Classification GCX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 22-18-0100
Product Code / EMDN: GCX
Device Name
Database Sync Date: 2026-08-09 09:00:32

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 VACUTRON?

The registered manufacturer of record for VACUTRON is Allied Medical, LLC.

What is the Primary UDI-DI identifier for VACUTRON?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 22-18-0100.

What classification code is assigned to this device?

This device is registered under product classification code GCX.

Similar Classification Devices (GCX)

Other Devices by Allied Medical, LLC

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