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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 — 7 UDI-DI variants, MDR (ACTEON MANUFACTURING)

MD Atlas
ACTEON MANUFACTURING

Data from EUDAMED, last updated May 19, 2026

EXPASYL

376024300expasyl27

7 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: 376024300expasyl27
Device name: EXPASYL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 1, 2022

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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FTTPGWDQHPNHND07ES6GMAM8

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

29410003760243000775
26100103760243007040
26101003760243007170
29923503760243007194
26101103760243007187
26103003760243007026
29401003760243007033