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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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Tubulures d'arthroscopie — 4 UDI-DI variants, MDR (HEMODIA SAS)

MD Atlas
HEMODIA SAS

Data from EUDAMED, last updated May 19, 2026

Tubulures d'arthroscopie

3661379FAB020002AEF

4 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: HEMODIA SAS

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Device characteristics

Animal tissues / cells

Identity & classification

Basic UDI-DI: 3661379FAB020002AEF
Device name: Tubulures d'arthroscopie
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 15, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K7KYBKQ41READ6TV0XC0G733

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

DOUBLEFLO Day Tube Set03661379223055
DOUBLEFLO OUTFLOW TUBE SET03661379223086
DOUBLEFLO PATIENT TUBE SET03661379223062
DOUBLEFLO Inflow Tube Set03661379223079