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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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Simeticone 250 mg — 4 UDI-DI variants, MDR (Fairpharm Vertriebs GmbH)

MD Atlas
Fairpharm Vertriebs GmbH

Data from EUDAMED, last updated May 23, 2026

Simeticone 250 mg

426075384E0605I01PX

4 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426075384E0605I01PX
Device name: Simeticone 250 mg
Device model: E0605I01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Oct 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: Fairpharm Vertriebs GmbH
SRN: DE-MF-000016959
Country: Germany
Email: info@fairpharm.com
Phone: +49 89 79102 0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K8N71HXN56FQR4GDRQG161CC

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

0426075384175604260753841756
0426075384146604260753841466
0426075384147304260753841473
0426075384148004260753841480