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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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2-Piece Urostomy Pouch — 6 UDI-DI variants, MDR (Dansac A/S)

MD Atlas
Dansac A/S

Data from EUDAMED, last updated May 23, 2026

2-Piece Urostomy Pouch

5709817D02P071S01104Q

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: Dansac A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5709817D02P071S01104Q
Device name: 2-Piece Urostomy Pouch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: Dansac A/S
SRN: DK-MF-000001514
Country: Denmark
Email: dansac@dansac.com
Phone: +45 4846 5100

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K59YZ4QAQ359RD7SSPH72F9V

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

Dansac05709817363470
Dansac05709817404302
Dansac05709817363449
Dansac05709817404333
Dansac05709817363500
Dansac05709817404272