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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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FLEXSOFT DUO — 4 UDI-DI variants, MDR (ORTHOSOFT)

MD Atlas
ORTHOSOFT

Data from EUDAMED, last updated May 19, 2026

FLEXSOFT DUO

37602703434015618358A

4 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: ORTHOSOFT

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37602703434015618358A
Device name: FLEXSOFT DUO
Device model: FLEXSOFT DUO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 6, 2022

Manufacturer & authorised representative

Manufacturer

Name: ORTHOSOFT
SRN: FR-MF-000000216
Country: France
Email: laurent.davoine@laboratoire-orthosoft.fr
Phone: +33 6 11 37 07 30

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01G0YY3YB583H6SSX9P8X69JDW

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

FD12D03760270340073
FD12G03760270340059
FD11G03760270340066
FD11D03760270340080