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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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Cuvette Clean — 2 UDI-DI variants, IVDR

MD Atlas
Human Gesellschaft für Biochemica und Diagnostica mbH

Data from EUDAMED, last updated May 23, 2026

Cuvette Clean

04033145CC18973FG

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: Human Gesellschaft für Biochemica und Diagnostica mbH

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 04033145CC18973FG
Device name: Cuvette Clean
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 25, 2024

Manufacturer & authorised representative

Manufacturer

Name: Human Gesellschaft für Biochemica und Diagnostica mbH
SRN: DE-MF-000025590
Country: Germany
Email: human@human.de
Phone: +49 6122 9988 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HWATS9Q0W67W8RT0B7NF5VJA

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

1897304033145179382
16663/2004033145131250