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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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Simeticon Vegacaps — 4 UDI-DI variants, MDR (Dr. Kleine Pharma GmbH)

MD Atlas
Dr. Kleine Pharma GmbH

Data from EUDAMED, last updated May 23, 2026

Simeticon Vegacaps

40395374446N

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: Dr. Kleine Pharma GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40395374446N
Device name: Simeticon Vegacaps
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Dec 20, 2024

Manufacturer & authorised representative

Manufacturer

Name: Dr. Kleine Pharma GmbH
SRN: DE-MF-000006589
Country: Germany
Email: info@kleine-pharma.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JFHETBD0ZYSM5MD2E0WJ8712

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

44404064761001658
44404064761001641
39134504064761002150
15001804064761001917