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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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LeucoScreen Plus — 5 UDI-DI variants, IVDR (FertiPro)

MD Atlas
FertiPro

Data from EUDAMED, last updated May 23, 2026

LeucoScreen Plus

5411967LEUCOP1ZP

5 UDI-DI variants

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

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

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 5411967LEUCOP1ZP
Device name: LeucoScreen Plus
Device model: LEUCO_PLUS
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: May 25, 2023

Manufacturer & authorised representative

Manufacturer

Name: FertiPro
SRN: BE-MF-000000313
Country: Belgium
Email: info@fertipro.com
Phone: +3250791805

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H191C7904B5DBZ5BMVC7K6SZ

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

LeucoScreen Plus05411967003020
LeucoScreen Plus Reagent 105411967003037
LeucoScreen Plus Reagent 205411967003044
LeucoScreen Plus Reagent 305411967003051
LeucoScreen Plus Reagent 405411967003068