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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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LOW SPEED CENTRIFUGES — 5 UDI-DI variants, IVDR

MD Atlas
Globe Scientific Europe B.V.

Data from EUDAMED, last updated May 31, 2026

LOW SPEED CENTRIFUGES

8721398269LOSPFW

5 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: Globe Scientific Europe B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8721398269LOSPFW
Device name: LOW SPEED CENTRIFUGES
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: Globe Scientific Europe B.V.
SRN: NL-MF-000046521
Country: Netherlands
Email: eumail@globescientific.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KN4GZSJ2V78220C3VKCAP3KY

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

Centrifuge, Clinical, Enhanced00840095674270
Centrifuge, Clinical, Enhanced00840095608381
Centrifuge, Clinical, Multi-Purpose, 240V00840095670616
Centrifuge, Clinical, Portable00840095681674
Centrifuge, Clinical, Standard00840095608398