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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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DiaCart 720g OP/F/C — 7 UDI-DI variants, MDR (Serumwerk Bernburg AG)

MD Atlas
Serumwerk Bernburg AG

Data from EUDAMED, last updated May 23, 2026

DiaCart 720g OP/F/C

426020097CARTRIDGE2K

7 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: Serumwerk Bernburg AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426020097CARTRIDGE2K
Device name: DiaCart 720g OP/F/C
Device model: Bicarbonate Cartridges for Haemodialysis
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jun 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: Serumwerk Bernburg AG
SRN: DE-MF-000005169
Country: Germany
Email: info@serumwerk.de
Phone: 03471860183

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01HZESXM1K72J05X0E2KJKNYEQ

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

150704260200971074
151404260200971081
151704260200970947
151304260200970930
150404260200971043
150504260200971050
152104260200970954