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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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Microlab 300 — 2 UDI-DI variants, IVDR (VitalScientific B.V. )

MD Atlas
VitalScientific B.V.

Data from EUDAMED, last updated May 31, 2026

Microlab 300

37017008Microlab-seriesHC

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: VitalScientific B.V.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 37017008Microlab-seriesHC
Device name: Microlab 300
Device model: 6002-310
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Oct 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: VitalScientific B.V.
SRN: NL-MF-000021018
Country: Netherlands
Email: a.intveld@vitalscientific.com
Phone: +31(0)313 430555

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K76S28J37N5NM8ZQSPWP8M4Z

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

6002-31003701700860037
6003-07503701700860266