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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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AV/721/SFR/22/R — 18 UDI-DI variants, MDR (Serumwerk Bernburg AG)

MD Atlas
Serumwerk Bernburg AG

Data from EUDAMED, last updated May 23, 2026

AV/721/SFR/22/R

426020097TUBINGSETEY

18 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: Serumwerk Bernburg AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426020097TUBINGSETEY
Device name: AV/721/SFR/22/R
Device model: Sterile Tubing Sets for Hemodialysis and Disposables
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 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

18 UDI-DI variants

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Applied filters

basicUdiUlid01J6VDVEZ2PRY2ZRGBR62KSTT3

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

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1745104260200971241
1705104260200971432
1432104260200971128
1434104260200971142
1481104260200971180
1741104260200971227
1744104260200971234
1744204260200971456
1473104260200971166
1411104260200971098
1472104260200971173
1484104260200971197
1412104260200971104
1436104260200971159
1746104260200971258
1433104260200971135
1704104260200971203