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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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Q-Pro 2000 — 6 UDI-DI variants, MDR (Meditec Medical Limited)

MD Atlas
Meditec Medical Limited

Data from EUDAMED, last updated May 24, 2026

Q-Pro 2000

539153749QPRO20018T

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Meditec Medical Limited

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 539153749QPRO20018T
Device name: Q-Pro 2000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: Meditec Medical Limited
SRN: IE-MF-000049210
Country: Ireland
Email: info@meditecmedical.com
Phone: +353(0)14624045

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K3KC0YRXG6CGAMKHG6SH18DY

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

QPro 2000 XT Mattress 4ft05391537490361
QPro 2000XT Mattress 3ft 6 inches wide05391537490354
QPro 2000XT Mattress 3ft Standard Size05391537490347
QPro 2000XT Mattress 4ft 6 inches05391537490378
QPro 2000XT Mattress 5ft05391537490385
QPro Alternating Chair Overlay05391537490392