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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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Centrifree Centrifugal Filter — 2 UDI-DI variants, IVDR

MD Atlas
Merck Millipore Ltd

Data from EUDAMED, last updated May 24, 2026

Centrifree Centrifugal Filter

40548441CSCTN

2 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: Merck Millipore Ltd

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 40548441CSCTN
Device name: Centrifree Centrifugal Filter
Device model: Centrifree
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: Merck Millipore Ltd
SRN: IE-MF-000003997
Country: Ireland
Email: PRRC_Cork@merckgroup.com
Phone: +35321488366

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JKAVBJ03M9M2RTPQ4QNM30YG

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

2198664312204061841767725
410404054839076046