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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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Benecura — 5 UDI-DI variants, MDR (Helmedica AG)

MD Atlas
Helmedica AG

Data from EUDAMED, last updated May 23, 2026

Benecura

7649990987BenecuraDJ

5 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: Helmedica AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7649990987BenecuraDJ
Device name: Benecura
Device model: Patienten-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: Jun 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: Helmedica AG
SRN: CH-MF-000040546
Country: Switzerland
Email: christian.schneider@helmedica.com
Phone: +41 44 515 8944

Authorised representative

Name: Axxos GmbH
SRN: DE-AR-000005590
Country: Germany
Phone: +41795637850

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J06DXCEJDGNEZXVQFY3NGP3X

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

2807649990987118
3207649990987156
2907649990987125
3107649990987149
3007649990987132