gudid Primary ID: WT920-B-MRI

MJM WOODTONE LINE (UDI WT920-B-MRI)

Manufactured by M J M International Corporation

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MJM WOODTONE LINE (Model/Catalog Number: WT920-B-MRI) is a medical device manufactured by M J M International Corporation. This product is indexed under FDA Product Code / Category Classification FPO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: WT920-B-MRI
Product Code / EMDN: FPO
Device Name
Database Sync Date: 2026-08-09 09:35:46

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 MJM WOODTONE LINE?

The registered manufacturer of record for MJM WOODTONE LINE is M J M International Corporation.

What is the Primary UDI-DI identifier for MJM WOODTONE LINE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is WT920-B-MRI.

What classification code is assigned to this device?

This device is registered under product classification code FPO.

Similar Classification Devices (FPO)

Other Devices by M J M International Corporation

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