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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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iPRESS — 2 UDI-DI variants, MDR (ELECTRONIQUE DU MAZET)

MD Atlas
ELECTRONIQUE DU MAZET

Data from EUDAMED, last updated May 19, 2026

iPRESS

137013302MEG009KP1XXXL

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: ELECTRONIQUE DU MAZET

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 137013302MEG009KP1XXXL
Device name: iPRESS
Device model: MEG009
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 16, 2022

Manufacturer & authorised representative

Manufacturer

Name: ELECTRONIQUE DU MAZET
SRN: FR-MF-000001805
Country: France
Email: contact@electroniquedumazet.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G4CZMAA862EWCZYX7DA0C8SR

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

iPress series 1003701330200135
iPress series 603701330200128