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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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Urine collection bag — 57 UDI-DI variants, MDR (Tecnoclínic SA)

MD Atlas
Tecnoclínic SA

Data from EUDAMED, last updated May 23, 2026

Urine collection bag

843657368BCONSTNG

57 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: 843657368BCONSTNG
Device name: Urine collection bag
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 21, 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

57 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G15DH8F520K47ZY863W4DNDM

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

29415-80015204046964503948
29435-80015304046964504044
29452R-80220804046955068005
29455-80219604046964504143
29451R-80220404046964842689
29411-80112604046964503924
29430-80112504046964504020

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