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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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PEDALE — 3 UDI-DI variants, MDR (HEMODIA SAS)

MD Atlas
HEMODIA SAS

Data from EUDAMED, last updated May 19, 2026

PEDALE

3661379FAB0400001E5

3 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: HEMODIA SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3661379FAB0400001E5
Device name: PEDALE
Device model: PEDALE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 16, 2023

Manufacturer & authorised representative

Manufacturer

Name: HEMODIA SAS
SRN: FR-MF-000007191
Country: France
Email: hemodia@hemodia.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GYHXCP46VY1D8JRN2SNED4YC

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

4-way pedal for "ArthroVims pump"03661379215432
Pédale 2 voies pour pompe AQUAVISION®03661379133361
Pédale 4 voies pour pompe AQUAVISION®03661379133378