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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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Instrument module MODULA — 5 UDI-DI variants, MDR

MD Atlas
G. Heinemann Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Instrument module MODULA

0426054893INC2S

5 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: G. Heinemann Medizintechnik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0426054893INC2S
Device name: Instrument module MODULA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: G. Heinemann Medizintechnik GmbH
SRN: DE-MF-000009705
Country: Germany
Email: info@heinemann-ent.de
Phone: +49 4191 95 379 0

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KMFPG991P7SPTAAHDHFTY2XY

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

Instrument module MODULA-HANSEAT L04260548932515
Instrument module MODULA-HANSEAT M04260548932539
Instrument module MODULA-HANSEAT XL04260548932522
Instrument module MODULA-ICL04260548932508
Instrument module MODULA-ICM04260548933505