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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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Helipur fresh — 2 UDI-DI variants, MDR (B. Braun Medical AG)

MD Atlas
B. Braun Medical AG

Data from EUDAMED, last updated May 31, 2026

Helipur fresh

40392390000032332D

2 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: B. Braun Medical AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40392390000032332D
Device name: Helipur fresh
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: B. Braun Medical AG
SRN: CH-MF-000017781
Country: Switzerland
Email: info.bbmch@bbraun.com
Phone: +41 58 258 50 00

Authorised representative

Name: B. Braun Melsungen AG
SRN: DE-AR-000000202
Country: Germany
Phone: +49 5661 71 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01KSSQ1JDDZ7377FNSA6NW0PS9

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

Helipur®04046955951826
Helipur®04046955951857