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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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Evolution 2 - 3 - 3e Tubing — 4 UDI-DI variants, MDR (Moria S.A.)

MD Atlas
Moria S.A.

Data from EUDAMED, last updated May 19, 2026

Evolution 2 - 3 - 3e Tubing

37004836TubingDV

4 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: Moria S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37004836TubingDV
Device name: Evolution 2 - 3 - 3e Tubing
Device model: 19138
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: Moria S.A.
SRN: FR-MF-000000336
Country: France
Email: pjay@moria-int.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K8QQA68Y38NTX5H885T11RVZ

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

ACP Tubing Set03700483620081
Evolution 2 - 3 - 3e Tubing03700483600243
Inflation Syringe and Tubing Set03700483602544
Infusion Tubing Set for Artif. Chamber03700483602162