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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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Expasyl Canules/cannulas — 5 UDI-DI variants, MDR

MD Atlas
ACTEON MANUFACTURING

Data from EUDAMED, last updated May 19, 2026

Expasyl Canules/cannulas

376024300expacanule7H

5 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: ACTEON MANUFACTURING

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376024300expacanule7H
Device name: Expasyl Canules/cannulas
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: ACTEON MANUFACTURING
SRN: FR-MF-000007556
Country: France
Email: genevieve.devilledon@acteongroup.com
Phone: +33 6 03 04 65 64

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FVMHWRMKKPQTKTMB1ANCXF1V

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

26100503760243000737
29402803760243000768
26101503760243000751
26104003760243000720
26104503760243000744