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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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ENT treatment unit MODULA — 6 UDI-DI variants, MDR

MD Atlas
Heinemann HNO Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

ENT treatment unit MODULA

0426251221MODW2

6 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: Heinemann HNO Medizintechnik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0426251221MODW2
Device name: ENT treatment unit MODULA
Device model: Duo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Heinemann HNO Medizintechnik GmbH
SRN: DE-MF-000046391
Country: Germany
Email: info@heinemann-ent.de
Phone: +49 4191 95 379 0

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KK1D71359TE9WRRJPN09GKKZ

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

ENT treatment unit MODULA Duo04262512210032
ENT treatment unit MODULA Europa04262512210025
ENT treatment unit MODULA L04262512210056
ENT treatment unit MODULA M04262512210049
ENT treatment unit MODULA Mini04262512210001
ENT treatment unit MODULA Paris04262512210018