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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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Q2K-03-Series — 3 UDI-DI variants, MDR (PRIME Medical Solutions)

MD Atlas
PRIME Medical Solutions

Data from EUDAMED, last updated May 23, 2026

Q2K-03-Series

540701054Q2K03TV

3 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: PRIME Medical Solutions

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 540701054Q2K03TV
Device name: Q2K-03-Series
Device model: Q2K-03-Series
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: PRIME Medical Solutions
SRN: BE-MF-000018858
Country: Belgium
Email: info@primemedicalsolutions.eu

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HEDV2KW4KATEWJ6705RM4R74

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

PQ2K032P0105407010540000
ProCell IV05407010540031
PQ2K033P0105407010540093