gudid Primary ID: Rack

Microvial rack 12/pkg (UDI Rack)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Microvial rack 12/pkg (Model/Catalog Number: Rack) is a medical device manufactured by M DIALYSIS INC.. This product is indexed under FDA Product Code / Category Classification GWM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Rack
Product Code / EMDN: GWM
Device Name
Database Sync Date: 2026-08-09 09:10:27

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 Microvial rack 12/pkg?

The registered manufacturer of record for Microvial rack 12/pkg is M DIALYSIS INC..

What is the Primary UDI-DI identifier for Microvial rack 12/pkg?

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

What classification code is assigned to this device?

This device is registered under product classification code GWM.

Similar Classification Devices (GWM)

Other Devices by M DIALYSIS INC.

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