gudid Primary ID: 1.34

HUMA (UDI 1.34)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The HUMA (Model/Catalog Number: 1.34) is a medical device manufactured by MedoPad Inc.. This product is indexed under FDA Product Code / Category Classification MWI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1.34
Product Code / EMDN: MWI
Device Name: The Huma platform is a modular Software as a Medical Device (SaMD) whichmay utilise compatible devices and software to obtain data collated via amobile app or web app and delivered to the clinician via a web portal or webapp where it may be viewed to drive clinical management. It is intended to beused for the physiological and non-physiological intermittent or spot-checkmonitoring of all condition patients in professional healthcare facilities, suchas clinics, hospitals or skilled nursing facilities, or in the patients homesetting. It is intended for the monitoring of patients by trained healthcareprofessionals.The Huma platform comprises a number of different modules andfunctionalities that can be selected by the customer for configuration of careplans which can be further personalised for the patients.Clinical information collected from these modules is displayed on a clinicianweb portal and patient app with the addition of flagging out of rangedatasets, trend visualisation, goal setting and communication channelsbetween clinicians and patients.
Database Sync Date: 2026-08-09 09:03:56

Full Regulatory Attributes

🔒 Token Gated

{
    "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 HUMA?

The registered manufacturer of record for HUMA is MedoPad Inc..

What is the Primary UDI-DI identifier for HUMA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.34.

What classification code is assigned to this device?

This device is registered under product classification code MWI.

Similar Classification Devices (MWI)

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