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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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MDPC-8127 — 4 UDI-DI variants, IVDR (Barco NV)

MD Atlas
Barco NV

Data from EUDAMED, last updated May 23, 2026

MDPC-8127

5415334_Patho-IVD_VT

4 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: Barco NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5415334_Patho-IVD_VT
Device name: MDPC-8127
Device model: Pathology Display
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: Barco NV
SRN: BE-MF-000000690
Country: Belgium
Email: eric.caus@barco.com
Phone: +3256233349

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JR7SBNMQ64SK3MX1MVYWEY4C

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

Barco05415334055919
Barco05415334055926
Barco05415334056244
Barco05415334056251