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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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Urinal - Men — 2 UDI-DI variants, MDR (MIXED.Industries B.V.)

MD Atlas
MIXED.Industries B.V.

Data from EUDAMED, last updated May 30, 2026

Urinal - Men

8719956880841JV

2 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: MIXED.Industries B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8719956880841JV
Device name: Urinal - Men
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 22, 2022

Manufacturer & authorised representative

Manufacturer

Name: MIXED.Industries B.V.
SRN: NL-MF-000006054
Country: Netherlands
Email: info@mixedindustries.nl
Phone: + 31 13 544 61 24

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GDJR1SX5GMNJN5V6FBS0T4E1

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

Urinal - Men87188859102614
Urinal - Women87188859102782