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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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Coudière — 5 UDI-DI variants, MDR (MEDISPORT)

MD Atlas
MEDISPORT

Data from EUDAMED, last updated May 19, 2026

Coudière

3664617CDE01QE

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: MEDISPORT

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3664617CDE01QE
Device name: Coudière
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: MEDISPORT
SRN: FR-MF-000000677
Country: France
Email: medifab@medisport.fr

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KQSCD4FQHM926HF0D6V85AZS

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

COUDIERE MDS03664617009398
COUDIERE MDS03664617009367
COUDIERE MDS03664617009350
COUDIERE MDS03664617009374
COUDIERE MDS03664617009381