3M (UDI CMW04)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The 3M (Model/Catalog Number: CMW04) is a medical device manufactured by 3M Deutschland GmbH. This product is indexed under FDA Product Code / Category Classification ITG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CMW04
Product Code / EMDN: ITG
Device Name: 3M Synthetic Cast Padding, CMW04, 4 inch x 4 yard (10cm x 3.6m), 20Roll/Bag, 4 Bags/Case
Database Sync Date: 2026-08-09 09:04:14

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 3M?

The registered manufacturer of record for 3M is 3M Deutschland GmbH.

What is the Primary UDI-DI identifier for 3M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CMW04.

What classification code is assigned to this device?

This device is registered under product classification code ITG.

Similar Classification Devices (ITG)

Other Devices by 3M Deutschland GmbH

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