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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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NIGHT URINE DRAINAGE BAG — 2 UDI-DI variants, MDR (Tecnoclínic SA)

MD Atlas
Tecnoclínic SA

Data from EUDAMED, last updated May 23, 2026

NIGHT URINE DRAINAGE BAG

843657368BCOURTMACSRS2

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: Tecnoclínic SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843657368BCOURTMACSRS2
Device name: NIGHT URINE DRAINAGE BAG
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 2, 2022

Manufacturer & authorised representative

Manufacturer

Name: Tecnoclínic SA
SRN: ES-MF-000000632
Country: Spain
Email: claracabal@tecnoclinic.com
Phone: +34 93 717 42 11

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G21R3H3S2ZGHGBPNJY116C57

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

5072FR-80709508436573680387
5072-80710708436573680813