gudid Primary ID: ManaCold Platinum Shoulder Pad

ManaMed (UDI ManaCold Platinum Shoulder Pad)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ManaMed (Model/Catalog Number: ManaCold Platinum Shoulder Pad) is a medical device manufactured by Manamed, Inc.. This product is indexed under FDA Product Code / Category Classification ILO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ManaCold Platinum Shoulder Pad
Product Code / EMDN: ILO
Device Name: ManaCold Platinum Shoulder Pad attachment is used decrease pain, swelling, and muscle spasms after surgery or injury. The cold therapy shoulder pad is applied to a patients injured area, delivering cold therapy through the ManaCold tubing and into the cold pad.Commonly used following shoulder surgery ManaCold Platinum Shoulder Pad can be used and operated by a patient or healthcare provider in a home or clinical setting
Database Sync Date: 2026-08-09 09:12:28

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 ManaMed?

The registered manufacturer of record for ManaMed is Manamed, Inc..

What is the Primary UDI-DI identifier for ManaMed?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ManaCold Platinum Shoulder Pad.

What classification code is assigned to this device?

This device is registered under product classification code ILO.

Similar Classification Devices (ILO)

Other Devices by Manamed, Inc.

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