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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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heat it App — 2 UDI-DI variants, MDR (Kamedi GmbH)

MD Atlas
Kamedi GmbH

Data from EUDAMED, last updated May 23, 2026

heat it App

4262370294669H

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Kamedi GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4262370294669H
Device name: heat it App
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: May 6, 2025

Manufacturer & authorised representative

Manufacturer

Name: Kamedi GmbH
SRN: DE-MF-000006270
Country: Germany
Email: info@heatit.de
Phone: +4972147044004

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JTJA0KM612YT69VSKCDMXAXY

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

heat it App for Android04262370290177
heat it App for iPhone04262370290184