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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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Centrifuge 5920R — 6 UDI-DI variants, IVDR (Eppendorf SE)

MD Atlas
Eppendorf SE

Data from EUDAMED, last updated May 23, 2026

Centrifuge 5920R

04043758-IA-CEN-010-NS

6 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Eppendorf SE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 04043758-IA-CEN-010-NS
Device name: Centrifuge 5920R
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jul 24, 2024

Manufacturer & authorised representative

Manufacturer

Name: Eppendorf SE
SRN: DE-MF-000006237
Country: Germany
Email: RA.Corporate@eppendorf.de

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01J3JA7JAB57MHNPE0KNA88GF3

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

5948 000.01804043758021749
5948 000.81604043758022128
5948 000.21204043758021817
5948 000.41704043758021930
5948 000.31004043758021879
5948 000.91404043758037139