gudid Primary ID: 415.1

TrenMAX (UDI 415.1)

Manufactured by Innovative Medical Products, Inc

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

Scannable UDI-DI Representation

Device Regulatory Overview

The TrenMAX (Model/Catalog Number: 415.1) is a medical device manufactured by Innovative Medical Products, Inc. This product is indexed under FDA Product Code / Category Classification FMP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 415.1
Product Code / EMDN: FMP
Device Name: Sample TrenMAX Pad
Database Sync Date: 2026-08-09 09:04:19

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 TrenMAX?

The registered manufacturer of record for TrenMAX is Innovative Medical Products, Inc.

What is the Primary UDI-DI identifier for TrenMAX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 415.1.

What classification code is assigned to this device?

This device is registered under product classification code FMP.

Similar Classification Devices (FMP)

Other Devices by Innovative Medical Products, Inc

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