gudid Primary ID: 6.M100-3.0/1

Humeca MAX Carrier 1:3 (UDI 6.M100-3.0/1)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Humeca MAX Carrier 1:3 (Model/Catalog Number: 6.M100-3.0/1) is a medical device manufactured by Humeca B.V.. This product is indexed under FDA Product Code / Category Classification MDM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 6.M100-3.0/1
Product Code / EMDN: MDM
Device Name
Database Sync Date: 2026-08-09 09:26:47

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 Humeca MAX Carrier 1:3?

The registered manufacturer of record for Humeca MAX Carrier 1:3 is Humeca B.V..

What is the Primary UDI-DI identifier for Humeca MAX Carrier 1:3?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6.M100-3.0/1.

What classification code is assigned to this device?

This device is registered under product classification code MDM.

Similar Classification Devices (MDM)

Other Devices by Humeca B.V.

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