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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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Minze Uroflow Accessories — 6 UDI-DI variants, MDR (Minze NV)

MD Atlas
Minze NV

Data from EUDAMED, last updated May 23, 2026

Minze Uroflow Accessories

5430000676944C

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: Minze NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5430000676944C
Device name: Minze Uroflow Accessories
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: Minze NV
SRN: BE-MF-000022123
Country: Belgium
Email: info@minzehealth.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JXHWKCJ2A3Y4BHGYT4MYR1Q5

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

Minze Homecup05430000676021
Minze Hospicup05430000676014
Minze Peehat05430000676045
Minze Potty05430000676120
Minze Shield05430000676052
Minze Standing Man Cup05430000676137